Canonical Allele Identifier: CA2495832689
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47412442_47412446delinsCAGAA , CM000664.2:g.47412442_47412446delinsCAGAA GRCh38
NC_000002.11:g.47639581_47639585delinsCAGAA , CM000664.1:g.47639581_47639585delinsCAGAA GRCh37
NC_000002.10:g.47493085_47493089delinsCAGAA NCBI36
NG_007110.2:g.14319_14323delinsCAGAA , LRG_218:g.14319_14323delinsCAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.674_678delinsCAGAA ENSP00000495641.2:p.Thr225=
ENST00000233146.7:c.674_678delinsCAGAA MANE Select ENSP00000233146.2:p.Thr225=
ENST00000543555.6:c.476_480delinsCAGAA ENSP00000442697.1:p.Thr159=
ENST00000644092.1:c.674_678delinsCAGAA ENSP00000496351.1:p.Thr225=
ENST00000645339.1:c.674_678delinsCAGAA ENSP00000496441.1:p.Thr225=
ENST00000645506.1:c.674_678delinsCAGAA ENSP00000495455.1:p.Thr225=
ENST00000646415.1:c.674_678delinsCAGAA ENSP00000495543.1:p.Thr225=
ENST00000233146.6:c.674_678delinsCAGAA ENSP00000233146.2:p.Thr225=
ENST00000406134.5:c.674_678delinsCAGAA ENSP00000384199.1:p.Thr225=
ENST00000543555.5:c.476_480delinsCAGAA ENSP00000442697.1:p.Thr159=
ENST00000610696.4:c.674_678delinsCAGAA ENSP00000483159.1:p.Thr225=
ENST00000613514.4:c.674_678delinsCAGAA ENSP00000484137.1:p.Thr225=
ENST00000617333.3:c.674_678delinsCAGAA ENSP00000482468.1:p.Thr225=
ENST00000617938.4:c.674_678delinsCAGAA ENSP00000481158.1:p.Thr225=
ENST00000621359.2:c.674_678delinsCAGAA ENSP00000481416.1:p.Thr225=
NM_000251.2:c.674_678delinsCAGAA , LRG_218t1:c.674_678delinsCAGAA NP_000242.1:p.Thr225=
NM_001258281.1:c.476_480delinsCAGAA NP_001245210.1:p.Thr159=
XM_005264332.2:c.674_678delinsCAGAA XP_005264389.2:p.Thr225=
XM_011532867.1:c.674_678delinsCAGAA XP_011531169.1:p.Thr225=
XR_939685.1:n.746_750delinsCAGAA
XM_005264332.4:c.674_678delinsCAGAA XP_005264389.2:p.Thr225=
XM_011532867.2:c.674_678delinsCAGAA XP_011531169.1:p.Thr225=
XR_001738747.2:n.736_740delinsCAGAA
XR_939685.2:n.736_740delinsCAGAA
NM_000251.3:c.674_678delinsCAGAA MANE Select NP_000242.1:p.Thr225=