Canonical Allele Identifier: CA366738137

Gene: PMS2

Linked Data

• dbSNP Id: rs2128704468
• MyVariant Identifiers: chr7:g.6022595G>C (hg19) ; chr7:g.5982964G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5982964G>C , CM000669.2:g.5982964G>C	GRCh38
NC_000007.13:g.6022595G>C , CM000669.1:g.6022595G>C	GRCh37
NC_000007.12:g.5989121G>C	NCBI36
NG_008466.1:g.31143C>G , LRG_161:g.31143C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1430C>G	ENSP00000514615.2:n.*1430C>G
ENST00000699840.2:c.2031C>G	ENSP00000514638.2:p.Ile677Met
ENST00000699930.2:c.1926C>G	ENSP00000514695.2:p.Ile642Met
ENST00000406569.8:c.1678+4123C>G	ENSP00000514464.1:n.1678+4123C>G
ENST00000644110.2:c.*1628C>G	ENSP00000496392.2:n.*1628C>G
ENST00000699752.1:c.1878C>G	ENSP00000514561.1:p.Ile626Met
ENST00000699753.1:c.*1455C>G	ENSP00000514562.1:n.*1455C>G
ENST00000699754.1:c.1836C>G	ENSP00000514563.1:p.Ile612Met
ENST00000699755.1:c.*1433C>G	ENSP00000514564.1:n.*1433C>G
ENST00000699756.1:c.*1621C>G	ENSP00000514565.1:n.*1621C>G
ENST00000699757.1:c.*1291C>G	ENSP00000514566.1:n.*1291C>G
ENST00000699758.1:c.*1291C>G	ENSP00000514567.1:n.*1291C>G
ENST00000699759.1:n.2888C>G
ENST00000699760.1:c.1716C>G	ENSP00000514568.1:p.Ile572Met
ENST00000699761.1:c.1629C>G	ENSP00000514569.1:p.Ile543Met
ENST00000699762.1:c.1461C>G	ENSP00000514570.1:p.Ile487Met
ENST00000699763.1:c.*1124C>G	ENSP00000514571.1:n.*1124C>G
ENST00000699764.1:c.*352C>G	ENSP00000514572.1:n.*352C>G
ENST00000699765.1:c.*1130C>G	ENSP00000514573.1:n.*1130C>G
ENST00000699766.1:c.2034C>G	ENSP00000514574.1:p.Ile678Met
ENST00000699767.1:c.2034C>G	ENSP00000514575.1:p.Ile678Met
ENST00000699768.1:c.2034C>G	ENSP00000514576.1:p.Ile678Met
ENST00000699811.1:c.1629C>G	ENSP00000514614.1:p.Ile543Met
ENST00000699813.1:n.2147C>G
ENST00000699814.1:c.1657C>G
ENST00000699815.1:c.*1565C>G	ENSP00000514616.1:n.*1565C>G
ENST00000699816.1:c.*924C>G	ENSP00000514617.1:n.*924C>G
ENST00000699817.1:c.*1628C>G	ENSP00000514618.1:n.*1628C>G
ENST00000699818.1:c.1629C>G	ENSP00000514619.1:p.Ile543Met
ENST00000699819.1:c.*1191C>G	ENSP00000514620.1:n.*1191C>G
ENST00000699820.1:c.1172C>G	ENSP00000514621.1:p.Ser391Ter
ENST00000699821.1:c.1629C>G	ENSP00000514622.1:p.Ile543Met
ENST00000699822.1:c.*1486C>G	ENSP00000514623.1:n.*1486C>G
ENST00000699823.1:c.1629C>G	ENSP00000514624.1:p.Ile543Met
ENST00000699824.1:c.*1537C>G	ENSP00000514625.1:n.*1537C>G
ENST00000699825.1:c.1473C>G	ENSP00000514626.1:p.Ile491Met
ENST00000699826.1:c.*1433C>G	ENSP00000514627.1:n.*1433C>G
ENST00000699827.1:c.1866C>G	ENSP00000514628.1:p.Ile622Met
ENST00000699828.1:c.*1124C>G	ENSP00000514629.1:n.*1124C>G
ENST00000699833.1:n.3806C>G
ENST00000699837.1:c.1629C>G	ENSP00000514635.1:p.Ile543Met
ENST00000699838.1:c.*1934C>G	ENSP00000514636.1:n.*1934C>G
ENST00000699839.1:c.2220C>G	ENSP00000514637.1:p.Ile740Met
ENST00000699916.1:c.*1291C>G	ENSP00000514684.1:n.*1291C>G
ENST00000699917.1:c.*1483C>G	ENSP00000514685.1:n.*1483C>G
ENST00000699918.1:c.*1535C>G	ENSP00000514686.1:n.*1535C>G
ENST00000699919.1:c.*1621C>G	ENSP00000514687.1:n.*1621C>G
ENST00000699920.1:c.*1670C>G	ENSP00000514688.1:n.*1670C>G
ENST00000699928.1:c.1016C>G	ENSP00000514693.1:p.Ser339Ter
ENST00000699951.1:c.*1130C>G	ENSP00000514706.1:n.*1130C>G
ENST00000699952.1:c.804-9422C>G	ENSP00000514707.1:n.804-9422C>G
ENST00000265849.12:c.2034C>G MANE Select	ENSP00000265849.7:p.Ile678Met
ENST00000642292.1:c.1629C>G	ENSP00000495524.1:p.Ile543Met
ENST00000642456.1:c.1629C>G	ENSP00000493814.1:p.Ile543Met
ENST00000643595.1:c.*1433C>G	ENSP00000494497.1:n.*1433C>G
ENST00000644110.1:c.1716C>G	ENSP00000496392.1:p.Ile572Met
ENST00000265849.11:c.2034C>G	ENSP00000265849.7:p.Ile678Met
ENST00000382321.5:c.831C>G	ENSP00000371758.4:p.Ile277Met
ENST00000406569.7:n.1678+4123C>G
ENST00000441476.6:c.1716C>G	ENSP00000392843.2:p.Ile572Met
ENST00000469652.1:n.63-59C>G
NM_000535.5:c.2034C>G , LRG_161t1:c.2034C>G	NP_000526.1:p.Ile678Met
NR_003085.2:n.2116C>G
XM_006715742.2:c.2028C>G	XP_006715805.1:p.Ile676Met
XM_006715744.2:c.1101C>G	XP_006715807.1:p.Ile367Met
XM_011515427.1:c.2079C>G	XP_011513729.1:p.Ile693Met
XM_011515428.1:c.1923C>G	XP_011513730.1:p.Ile641Met
XM_011515429.1:c.1716C>G	XP_011513731.1:p.Ile572Met
XM_011515430.1:c.1716C>G	XP_011513732.1:p.Ile572Met
NM_000535.6:c.2034C>G	NP_000526.2:p.Ile678Met
NM_001322003.1:c.1629C>G	NP_001308932.1:p.Ile543Met
NM_001322004.1:c.1629C>G	NP_001308933.1:p.Ile543Met
NM_001322005.1:c.1629C>G	NP_001308934.1:p.Ile543Met
NM_001322006.1:c.1878C>G	NP_001308935.1:p.Ile626Met
NM_001322007.1:c.1716C>G	NP_001308936.1:p.Ile572Met
NM_001322008.1:c.1716C>G	NP_001308937.1:p.Ile572Met
NM_001322009.1:c.1629C>G	NP_001308938.1:p.Ile543Met
NM_001322010.1:c.1473C>G	NP_001308939.1:p.Ile491Met
NM_001322011.1:c.1101C>G	NP_001308940.1:p.Ile367Met
NM_001322012.1:c.1101C>G	NP_001308941.1:p.Ile367Met
NM_001322013.1:c.1461C>G	NP_001308942.1:p.Ile487Met
NM_001322014.1:c.2034C>G	NP_001308943.1:p.Ile678Met
NM_001322015.1:c.1725C>G	NP_001308944.1:p.Ile575Met
NR_136154.1:n.2121C>G
XM_006715744.4:c.1101C>G	XP_006715807.1:p.Ile367Met
XM_017012342.2:c.1101C>G	XP_016867831.1:p.Ile367Met
XM_024446800.1:c.1473C>G	XP_024302568.1:p.Ile491Met
NM_000535.7:c.2034C>G MANE Select	NP_000526.2:p.Ile678Met
NM_001322003.2:c.1629C>G	NP_001308932.1:p.Ile543Met
NM_001322004.2:c.1629C>G	NP_001308933.1:p.Ile543Met
NM_001322005.2:c.1629C>G	NP_001308934.1:p.Ile543Met
NM_001322006.2:c.1878C>G	NP_001308935.1:p.Ile626Met
NM_001322008.2:c.1716C>G	NP_001308937.1:p.Ile572Met
NM_001322009.2:c.1629C>G	NP_001308938.1:p.Ile543Met
NM_001322010.2:c.1473C>G	NP_001308939.1:p.Ile491Met
NM_001322011.2:c.1101C>G	NP_001308940.1:p.Ile367Met
NM_001322012.2:c.1101C>G	NP_001308941.1:p.Ile367Met
NM_001322013.2:c.1461C>G	NP_001308942.1:p.Ile487Met
NM_001322014.2:c.2034C>G	NP_001308943.1:p.Ile678Met
NM_001322015.2:c.1725C>G	NP_001308944.1:p.Ile575Met
NM_001322007.2:c.1716C>G	NP_001308936.1:p.Ile572Met