Canonical Allele Identifier: CA2495872585

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475250_47475251delinsAG , CM000664.2:g.47475250_47475251delinsAG	GRCh38
NC_000002.11:g.47702389_47702390delinsAG , CM000664.1:g.47702389_47702390delinsAG	GRCh37
NC_000002.10:g.47555893_47555894delinsAG	NCBI36
NG_007110.2:g.77127_77128delinsAG , LRG_218:g.77127_77128delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1985_1986delinsAG	ENSP00000495641.2:p.Gln662=
ENST00000233146.7:c.1985_1986delinsAG MANE Select	ENSP00000233146.2:p.Gln662=
ENST00000543555.6:c.1787_1788delinsAG	ENSP00000442697.1:p.Gln596=
ENST00000644092.1:c.*285_*286delinsAG	ENSP00000496351.1:n.*285_*286delinsAG
ENST00000645339.1:c.1985_1986delinsAG	ENSP00000496441.1:p.Gln662=
ENST00000645506.1:c.1985_1986delinsAG	ENSP00000495455.1:p.Gln662=
ENST00000646415.1:c.1985_1986delinsAG	ENSP00000495543.1:p.Gln662=
ENST00000233146.6:c.1985_1986delinsAG	ENSP00000233146.2:p.Gln662=
ENST00000406134.5:c.1985_1986delinsAG	ENSP00000384199.1:p.Gln662=
ENST00000543555.5:c.1787_1788delinsAG	ENSP00000442697.1:p.Gln596=
ENST00000610696.4:c.*381_*382delinsAG	ENSP00000483159.1:n.*381_*382delinsAG
ENST00000613514.4:c.*525_*526delinsAG	ENSP00000484137.1:n.*525_*526delinsAG
ENST00000617333.3:c.*751_*752delinsAG	ENSP00000482468.1:n.*751_*752delinsAG
ENST00000617938.4:c.*957_*958delinsAG	ENSP00000481158.1:n.*957_*958delinsAG
ENST00000621359.2:c.1985_1986delinsAG	ENSP00000481416.1:p.Gln662=
NM_000251.2:c.1985_1986delinsAG , LRG_218t1:c.1985_1986delinsAG	NP_000242.1:p.Gln662=
NM_001258281.1:c.1787_1788delinsAG	NP_001245210.1:p.Gln596=
XM_005264332.2:c.1985_1986delinsAG	XP_005264389.2:p.Gln662=
XM_011532867.1:c.1985_1986delinsAG	XP_011531169.1:p.Gln662=
XR_939685.1:n.2057_2058delinsAG
XM_005264332.4:c.1985_1986delinsAG	XP_005264389.2:p.Gln662=
XM_011532867.2:c.1985_1986delinsAG	XP_011531169.1:p.Gln662=
XR_001738747.2:n.2047_2048delinsAG
XR_939685.2:n.2047_2048delinsAG
NM_000251.3:c.1985_1986delinsAG MANE Select	NP_000242.1:p.Gln662=