Canonical Allele Identifier: CA453643230

Gene: PMS2

Linked Data

• MyVariant Identifiers: chr7:g.6022523G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5982892G>C , CM000669.2:g.5982892G>C	GRCh38
NC_000007.13:g.6022523G>C , CM000669.1:g.6022523G>C	GRCh37
NC_000007.12:g.5989049G>C	NCBI36
NG_008466.1:g.31215C>G , LRG_161:g.31215C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000699814.2:c.*1502C>G	ENSP00000514615.2:n.*1502C>G
ENST00000699840.2:c.2103C>G	ENSP00000514638.2:p.Ala701=
ENST00000699930.2:c.1998C>G	ENSP00000514695.2:p.Ala666=
ENST00000406569.8:c.1678+4195C>G	ENSP00000514464.1:n.1678+4195C>G
ENST00000644110.2:c.*1700C>G	ENSP00000496392.2:n.*1700C>G
ENST00000699752.1:c.1950C>G	ENSP00000514561.1:p.Ala650=
ENST00000699753.1:c.*1527C>G	ENSP00000514562.1:n.*1527C>G
ENST00000699754.1:c.1908C>G	ENSP00000514563.1:p.Ala636=
ENST00000699755.1:c.*1505C>G	ENSP00000514564.1:n.*1505C>G
ENST00000699756.1:c.*1693C>G	ENSP00000514565.1:n.*1693C>G
ENST00000699757.1:c.*1363C>G	ENSP00000514566.1:n.*1363C>G
ENST00000699758.1:c.*1363C>G	ENSP00000514567.1:n.*1363C>G
ENST00000699759.1:n.2960C>G
ENST00000699760.1:c.1788C>G	ENSP00000514568.1:p.Ala596=
ENST00000699761.1:c.1701C>G	ENSP00000514569.1:p.Ala567=
ENST00000699762.1:c.1533C>G	ENSP00000514570.1:p.Ala511=
ENST00000699763.1:c.*1196C>G	ENSP00000514571.1:n.*1196C>G
ENST00000699764.1:c.*424C>G	ENSP00000514572.1:n.*424C>G
ENST00000699765.1:c.*1202C>G	ENSP00000514573.1:n.*1202C>G
ENST00000699766.1:c.2106C>G	ENSP00000514574.1:p.Ala702=
ENST00000699767.1:c.2106C>G	ENSP00000514575.1:p.Ala702=
ENST00000699768.1:c.2106C>G	ENSP00000514576.1:p.Ala702=
ENST00000699811.1:c.1701C>G	ENSP00000514614.1:p.Ala567=
ENST00000699813.1:n.2219C>G
ENST00000699814.1:c.1729C>G
ENST00000699815.1:c.*1637C>G	ENSP00000514616.1:n.*1637C>G
ENST00000699816.1:c.*996C>G	ENSP00000514617.1:n.*996C>G
ENST00000699817.1:c.*1700C>G	ENSP00000514618.1:n.*1700C>G
ENST00000699818.1:c.1701C>G	ENSP00000514619.1:p.Ala567=
ENST00000699819.1:c.*1263C>G	ENSP00000514620.1:n.*1263C>G
ENST00000699820.1:c.*44C>G	ENSP00000514621.1:n.*44C>G
ENST00000699821.1:c.1701C>G	ENSP00000514622.1:p.Ala567=
ENST00000699822.1:c.*1558C>G	ENSP00000514623.1:n.*1558C>G
ENST00000699823.1:c.1701C>G	ENSP00000514624.1:p.Ala567=
ENST00000699824.1:c.*1609C>G	ENSP00000514625.1:n.*1609C>G
ENST00000699825.1:c.1545C>G	ENSP00000514626.1:p.Ala515=
ENST00000699826.1:c.*1505C>G	ENSP00000514627.1:n.*1505C>G
ENST00000699827.1:c.1938C>G	ENSP00000514628.1:p.Ala646=
ENST00000699828.1:c.*1196C>G	ENSP00000514629.1:n.*1196C>G
ENST00000699833.1:n.3878C>G
ENST00000699837.1:c.1701C>G	ENSP00000514635.1:p.Ala567=
ENST00000699838.1:c.*2006C>G	ENSP00000514636.1:n.*2006C>G
ENST00000699839.1:c.2292C>G	ENSP00000514637.1:p.Ala764=
ENST00000699916.1:c.*1363C>G	ENSP00000514684.1:n.*1363C>G
ENST00000699917.1:c.*1555C>G	ENSP00000514685.1:n.*1555C>G
ENST00000699918.1:c.*1607C>G	ENSP00000514686.1:n.*1607C>G
ENST00000699919.1:c.*1693C>G	ENSP00000514687.1:n.*1693C>G
ENST00000699920.1:c.*1742C>G	ENSP00000514688.1:n.*1742C>G
ENST00000699928.1:c.*44C>G	ENSP00000514693.1:n.*44C>G
ENST00000699951.1:c.*1202C>G	ENSP00000514706.1:n.*1202C>G
ENST00000699952.1:c.804-9350C>G	ENSP00000514707.1:n.804-9350C>G
ENST00000265849.12:c.2106C>G MANE Select	ENSP00000265849.7:p.Ala702=
ENST00000642292.1:c.1701C>G	ENSP00000495524.1:p.Ala567=
ENST00000642456.1:c.1701C>G	ENSP00000493814.1:p.Ala567=
ENST00000643595.1:c.*1505C>G	ENSP00000494497.1:n.*1505C>G
ENST00000644110.1:c.1788C>G	ENSP00000496392.1:p.Ala596=
ENST00000265849.11:c.2106C>G	ENSP00000265849.7:p.Ala702=
ENST00000382321.5:c.903C>G	ENSP00000371758.4:p.Ala301=
ENST00000406569.7:n.1678+4195C>G
ENST00000441476.6:c.1788C>G	ENSP00000392843.2:p.Ala596=
ENST00000469652.1:n.76C>G
NM_000535.5:c.2106C>G , LRG_161t1:c.2106C>G	NP_000526.1:p.Ala702=
NR_003085.2:n.2188C>G
XM_006715742.2:c.2100C>G	XP_006715805.1:p.Ala700=
XM_006715744.2:c.1173C>G	XP_006715807.1:p.Ala391=
XM_011515427.1:c.2151C>G	XP_011513729.1:p.Ala717=
XM_011515428.1:c.1995C>G	XP_011513730.1:p.Ala665=
XM_011515429.1:c.1788C>G	XP_011513731.1:p.Ala596=
XM_011515430.1:c.1788C>G	XP_011513732.1:p.Ala596=
NM_000535.6:c.2106C>G	NP_000526.2:p.Ala702=
NM_001322003.1:c.1701C>G	NP_001308932.1:p.Ala567=
NM_001322004.1:c.1701C>G	NP_001308933.1:p.Ala567=
NM_001322005.1:c.1701C>G	NP_001308934.1:p.Ala567=
NM_001322006.1:c.1950C>G	NP_001308935.1:p.Ala650=
NM_001322007.1:c.1788C>G	NP_001308936.1:p.Ala596=
NM_001322008.1:c.1788C>G	NP_001308937.1:p.Ala596=
NM_001322009.1:c.1701C>G	NP_001308938.1:p.Ala567=
NM_001322010.1:c.1545C>G	NP_001308939.1:p.Ala515=
NM_001322011.1:c.1173C>G	NP_001308940.1:p.Ala391=
NM_001322012.1:c.1173C>G	NP_001308941.1:p.Ala391=
NM_001322013.1:c.1533C>G	NP_001308942.1:p.Ala511=
NM_001322014.1:c.2106C>G	NP_001308943.1:p.Ala702=
NM_001322015.1:c.1797C>G	NP_001308944.1:p.Ala599=
NR_136154.1:n.2193C>G
XM_006715744.4:c.1173C>G	XP_006715807.1:p.Ala391=
XM_017012342.2:c.1173C>G	XP_016867831.1:p.Ala391=
XM_024446800.1:c.1545C>G	XP_024302568.1:p.Ala515=
NM_000535.7:c.2106C>G MANE Select	NP_000526.2:p.Ala702=
NM_001322003.2:c.1701C>G	NP_001308932.1:p.Ala567=
NM_001322004.2:c.1701C>G	NP_001308933.1:p.Ala567=
NM_001322005.2:c.1701C>G	NP_001308934.1:p.Ala567=
NM_001322006.2:c.1950C>G	NP_001308935.1:p.Ala650=
NM_001322008.2:c.1788C>G	NP_001308937.1:p.Ala596=
NM_001322009.2:c.1701C>G	NP_001308938.1:p.Ala567=
NM_001322010.2:c.1545C>G	NP_001308939.1:p.Ala515=
NM_001322011.2:c.1173C>G	NP_001308940.1:p.Ala391=
NM_001322012.2:c.1173C>G	NP_001308941.1:p.Ala391=
NM_001322013.2:c.1533C>G	NP_001308942.1:p.Ala511=
NM_001322014.2:c.2106C>G	NP_001308943.1:p.Ala702=
NM_001322015.2:c.1797C>G	NP_001308944.1:p.Ala599=
NM_001322007.2:c.1788C>G	NP_001308936.1:p.Ala596=