Canonical Allele Identifier: CA2495872466
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47475118_47475122delinsCATAT , CM000664.2:g.47475118_47475122delinsCATAT GRCh38
NC_000002.11:g.47702257_47702261delinsCATAT , CM000664.1:g.47702257_47702261delinsCATAT GRCh37
NC_000002.10:g.47555761_47555765delinsCATAT NCBI36
NG_007110.2:g.76995_76999delinsCATAT , LRG_218:g.76995_76999delinsCATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.1853_1857delinsCATAT ENSP00000495641.2:p.Pro618=
ENST00000233146.7:c.1853_1857delinsCATAT MANE Select ENSP00000233146.2:p.Pro618=
ENST00000543555.6:c.1655_1659delinsCATAT ENSP00000442697.1:p.Pro552=
ENST00000644092.1:c.*153_*157delinsCATAT ENSP00000496351.1:n.*153_*157delinsCATAT
ENST00000645339.1:c.1853_1857delinsCATAT ENSP00000496441.1:p.Pro618=
ENST00000645506.1:c.1853_1857delinsCATAT ENSP00000495455.1:p.Pro618=
ENST00000646415.1:c.1853_1857delinsCATAT ENSP00000495543.1:p.Pro618=
ENST00000233146.6:c.1853_1857delinsCATAT ENSP00000233146.2:p.Pro618=
ENST00000406134.5:c.1853_1857delinsCATAT ENSP00000384199.1:p.Pro618=
ENST00000543555.5:c.1655_1659delinsCATAT ENSP00000442697.1:p.Pro552=
ENST00000610696.4:c.*249_*253delinsCATAT ENSP00000483159.1:n.*249_*253delinsCATAT
ENST00000613514.4:c.*393_*397delinsCATAT ENSP00000484137.1:n.*393_*397delinsCATAT
ENST00000617333.3:c.*619_*623delinsCATAT ENSP00000482468.1:n.*619_*623delinsCATAT
ENST00000617938.4:c.*825_*829delinsCATAT ENSP00000481158.1:n.*825_*829delinsCATAT
ENST00000621359.2:c.1853_1857delinsCATAT ENSP00000481416.1:p.Pro618=
NM_000251.2:c.1853_1857delinsCATAT , LRG_218t1:c.1853_1857delinsCATAT NP_000242.1:p.Pro618=
NM_001258281.1:c.1655_1659delinsCATAT NP_001245210.1:p.Pro552=
XM_005264332.2:c.1853_1857delinsCATAT XP_005264389.2:p.Pro618=
XM_011532867.1:c.1853_1857delinsCATAT XP_011531169.1:p.Pro618=
XR_939685.1:n.1925_1929delinsCATAT
XM_005264332.4:c.1853_1857delinsCATAT XP_005264389.2:p.Pro618=
XM_011532867.2:c.1853_1857delinsCATAT XP_011531169.1:p.Pro618=
XR_001738747.2:n.1915_1919delinsCATAT
XR_939685.2:n.1915_1919delinsCATAT
NM_000251.3:c.1853_1857delinsCATAT MANE Select NP_000242.1:p.Pro618=