Canonical Allele Identifier: CA2495876034
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47480721_47480722delinsTC , CM000664.2:g.47480721_47480722delinsTC GRCh38
NC_000002.11:g.47707860_47707861delinsTC , CM000664.1:g.47707860_47707861delinsTC GRCh37
NC_000002.10:g.47561364_47561365delinsTC NCBI36
NG_007110.2:g.82598_82599delinsTC , LRG_218:g.82598_82599delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.2484_2485delinsTC ENSP00000495641.2:p.Ile828=
ENST00000233146.7:c.2484_2485delinsTC MANE Select ENSP00000233146.2:p.Ile828=
ENST00000543555.6:c.2286_2287delinsTC ENSP00000442697.1:p.Ile762=
ENST00000644092.1:c.*784_*785delinsTC ENSP00000496351.1:n.*784_*785delinsTC
ENST00000644900.1:c.337_338delinsTC
ENST00000645339.1:c.2484_2485delinsTC ENSP00000496441.1:p.Ile828=
ENST00000645506.1:c.2484_2485delinsTC ENSP00000495455.1:p.Ile828=
ENST00000646415.1:c.2484_2485delinsTC ENSP00000495543.1:p.Ile828=
ENST00000233146.6:c.2484_2485delinsTC ENSP00000233146.2:p.Ile828=
ENST00000406134.5:c.2484_2485delinsTC ENSP00000384199.1:p.Ile828=
ENST00000543555.5:c.2286_2287delinsTC ENSP00000442697.1:p.Ile762=
ENST00000610696.4:c.*880_*881delinsTC ENSP00000483159.1:n.*880_*881delinsTC
ENST00000613514.4:c.*1024_*1025delinsTC ENSP00000484137.1:n.*1024_*1025delinsTC
ENST00000617333.3:c.*1250_*1251delinsTC ENSP00000482468.1:n.*1250_*1251delinsTC
ENST00000617938.4:c.*1456_*1457delinsTC ENSP00000481158.1:n.*1456_*1457delinsTC
ENST00000621359.2:c.*50_*51delinsTC ENSP00000481416.1:n.*50_*51delinsTC
NM_000251.2:c.2484_2485delinsTC , LRG_218t1:c.2484_2485delinsTC NP_000242.1:p.Ile828=
NM_001258281.1:c.2286_2287delinsTC NP_001245210.1:p.Ile762=
XM_005264332.2:c.2484_2485delinsTC XP_005264389.2:p.Ile828=
XM_011532867.1:c.2484_2485delinsTC XP_011531169.1:p.Ile828=
XR_939685.1:n.2556_2557delinsTC
XM_005264332.4:c.2484_2485delinsTC XP_005264389.2:p.Ile828=
XM_011532867.2:c.2484_2485delinsTC XP_011531169.1:p.Ile828=
XR_001738747.2:n.2546_2547delinsTC
XR_939685.2:n.2546_2547delinsTC
NM_000251.3:c.2484_2485delinsTC MANE Select NP_000242.1:p.Ile828=