Canonical Allele Identifier: CA366735531

Gene: PMS2

Linked Data

• dbSNP Id: rs587779338
• MyVariant Identifiers: chr7:g.6017220G>C (hg19) ; chr7:g.5977589G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5977589G>C , CM000669.2:g.5977589G>C	GRCh38
NC_000007.13:g.6017220G>C , CM000669.1:g.6017220G>C	GRCh37
NC_000007.12:g.5983746G>C	NCBI36
NG_008466.1:g.36518C>G , LRG_161:g.36518C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1840C>G	ENSP00000514615.2:n.*1840C>G
ENST00000699840.2:c.2441C>G	ENSP00000514638.2:p.Ser814Trp
ENST00000699930.2:c.2336C>G	ENSP00000514695.2:p.Ser779Trp
ENST00000406569.8:c.1804C>G	ENSP00000514464.1:n.1804C>G
ENST00000644110.2:c.*2038C>G	ENSP00000496392.2:n.*2038C>G
ENST00000699752.1:c.2288C>G	ENSP00000514561.1:p.Ser763Trp
ENST00000699753.1:c.*1865C>G	ENSP00000514562.1:n.*1865C>G
ENST00000699754.1:c.2246C>G	ENSP00000514563.1:p.Ser749Trp
ENST00000699755.1:c.*1843C>G	ENSP00000514564.1:n.*1843C>G
ENST00000699756.1:c.*2031C>G	ENSP00000514565.1:n.*2031C>G
ENST00000699757.1:c.*1701C>G	ENSP00000514566.1:n.*1701C>G
ENST00000699758.1:c.*1701C>G	ENSP00000514567.1:n.*1701C>G
ENST00000699759.1:n.3298C>G
ENST00000699760.1:c.2126C>G	ENSP00000514568.1:p.Ser709Trp
ENST00000699761.1:c.2039C>G	ENSP00000514569.1:p.Ser680Trp
ENST00000699762.1:c.1871C>G	ENSP00000514570.1:p.Ser624Trp
ENST00000699763.1:c.*1534C>G	ENSP00000514571.1:n.*1534C>G
ENST00000699764.1:c.*762C>G	ENSP00000514572.1:n.*762C>G
ENST00000699765.1:c.*1439C>G	ENSP00000514573.1:n.*1439C>G
ENST00000699766.1:c.2477C>G	ENSP00000514574.1:p.Ser826Trp
ENST00000699767.1:c.*85C>G	ENSP00000514575.1:n.*85C>G
ENST00000699768.1:c.2300C>G	ENSP00000514576.1:p.Ser767Trp
ENST00000699811.1:c.2039C>G	ENSP00000514614.1:p.Ser680Trp
ENST00000699813.1:n.2557C>G
ENST00000699814.1:c.2067C>G
ENST00000699815.1:c.*1975C>G	ENSP00000514616.1:n.*1975C>G
ENST00000699816.1:c.*1334C>G	ENSP00000514617.1:n.*1334C>G
ENST00000699817.1:c.*2038C>G	ENSP00000514618.1:n.*2038C>G
ENST00000699818.1:c.2039C>G	ENSP00000514619.1:p.Ser680Trp
ENST00000699819.1:c.*1601C>G	ENSP00000514620.1:n.*1601C>G
ENST00000699820.1:c.*382C>G	ENSP00000514621.1:n.*382C>G
ENST00000699821.1:c.2072C>G	ENSP00000514622.1:p.Ser691Trp
ENST00000699822.1:c.*1896C>G	ENSP00000514623.1:n.*1896C>G
ENST00000699823.1:c.2039C>G	ENSP00000514624.1:p.Ser680Trp
ENST00000699824.1:c.*1947C>G	ENSP00000514625.1:n.*1947C>G
ENST00000699825.1:c.1883C>G	ENSP00000514626.1:p.Ser628Trp
ENST00000699826.1:c.*1843C>G	ENSP00000514627.1:n.*1843C>G
ENST00000699827.1:c.2276C>G	ENSP00000514628.1:p.Ser759Trp
ENST00000699828.1:c.*1534C>G	ENSP00000514629.1:n.*1534C>G
ENST00000699833.1:n.4216C>G
ENST00000699837.1:c.2039C>G	ENSP00000514635.1:p.Ser680Trp
ENST00000699838.1:c.*2344C>G	ENSP00000514636.1:n.*2344C>G
ENST00000699839.1:c.2630C>G	ENSP00000514637.1:p.Ser877Trp
ENST00000699916.1:c.*1701C>G	ENSP00000514684.1:n.*1701C>G
ENST00000699917.1:c.*1893C>G	ENSP00000514685.1:n.*1893C>G
ENST00000699918.1:c.*1945C>G	ENSP00000514686.1:n.*1945C>G
ENST00000699919.1:c.*2031C>G	ENSP00000514687.1:n.*2031C>G
ENST00000699920.1:c.*2080C>G	ENSP00000514688.1:n.*2080C>G
ENST00000699928.1:c.*382C>G	ENSP00000514693.1:n.*382C>G
ENST00000699951.1:c.*1497C>G	ENSP00000514706.1:n.*1497C>G
ENST00000699952.1:c.804-4047C>G	ENSP00000514707.1:n.804-4047C>G
ENST00000265849.12:c.2444C>G MANE Select	ENSP00000265849.7:p.Ser815Trp
ENST00000642292.1:c.2039C>G	ENSP00000495524.1:p.Ser680Trp
ENST00000642456.1:c.2039C>G	ENSP00000493814.1:p.Ser680Trp
ENST00000643595.1:c.*1843C>G	ENSP00000494497.1:n.*1843C>G
ENST00000644110.1:c.2126C>G	ENSP00000496392.1:p.Ser709Trp
ENST00000265849.11:c.2444C>G	ENSP00000265849.7:p.Ser815Trp
ENST00000382321.5:c.1241C>G	ENSP00000371758.4:p.Ser414Trp
ENST00000441476.6:c.2126C>G	ENSP00000392843.2:p.Ser709Trp
NM_000535.5:c.2444C>G , LRG_161t1:c.2444C>G	NP_000526.1:p.Ser815Trp
NR_003085.2:n.2526C>G
XM_006715742.2:c.2438C>G	XP_006715805.1:p.Ser813Trp
XM_006715744.2:c.1511C>G	XP_006715807.1:p.Ser504Trp
XM_011515427.1:c.2489C>G	XP_011513729.1:p.Ser830Trp
XM_011515428.1:c.2333C>G	XP_011513730.1:p.Ser778Trp
XM_011515429.1:c.2126C>G	XP_011513731.1:p.Ser709Trp
XM_011515430.1:c.2126C>G	XP_011513732.1:p.Ser709Trp
NM_000535.6:c.2444C>G	NP_000526.2:p.Ser815Trp
NM_001322003.1:c.2039C>G	NP_001308932.1:p.Ser680Trp
NM_001322004.1:c.2039C>G	NP_001308933.1:p.Ser680Trp
NM_001322005.1:c.2039C>G	NP_001308934.1:p.Ser680Trp
NM_001322006.1:c.2288C>G	NP_001308935.1:p.Ser763Trp
NM_001322007.1:c.2126C>G	NP_001308936.1:p.Ser709Trp
NM_001322008.1:c.2126C>G	NP_001308937.1:p.Ser709Trp
NM_001322009.1:c.2072C>G	NP_001308938.1:p.Ser691Trp
NM_001322010.1:c.1883C>G	NP_001308939.1:p.Ser628Trp
NM_001322011.1:c.1511C>G	NP_001308940.1:p.Ser504Trp
NM_001322012.1:c.1511C>G	NP_001308941.1:p.Ser504Trp
NM_001322013.1:c.1871C>G	NP_001308942.1:p.Ser624Trp
NM_001322014.1:c.2477C>G	NP_001308943.1:p.Ser826Trp
NM_001322015.1:c.2135C>G	NP_001308944.1:p.Ser712Trp
NR_136154.1:n.2488C>G
XM_006715744.4:c.1511C>G	XP_006715807.1:p.Ser504Trp
XM_017012342.2:c.1511C>G	XP_016867831.1:p.Ser504Trp
XM_024446800.1:c.1883C>G	XP_024302568.1:p.Ser628Trp
NM_000535.7:c.2444C>G MANE Select	NP_000526.2:p.Ser815Trp
NM_001322003.2:c.2039C>G	NP_001308932.1:p.Ser680Trp
NM_001322004.2:c.2039C>G	NP_001308933.1:p.Ser680Trp
NM_001322005.2:c.2039C>G	NP_001308934.1:p.Ser680Trp
NM_001322006.2:c.2288C>G	NP_001308935.1:p.Ser763Trp
NM_001322008.2:c.2126C>G	NP_001308937.1:p.Ser709Trp
NM_001322009.2:c.2072C>G	NP_001308938.1:p.Ser691Trp
NM_001322010.2:c.1883C>G	NP_001308939.1:p.Ser628Trp
NM_001322011.2:c.1511C>G	NP_001308940.1:p.Ser504Trp
NM_001322012.2:c.1511C>G	NP_001308941.1:p.Ser504Trp
NM_001322013.2:c.1871C>G	NP_001308942.1:p.Ser624Trp
NM_001322014.2:c.2477C>G	NP_001308943.1:p.Ser826Trp
NM_001322015.2:c.2135C>G	NP_001308944.1:p.Ser712Trp
NM_001322007.2:c.2126C>G	NP_001308936.1:p.Ser709Trp