Canonical Allele Identifier: CA2495877344

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482873_47482874delinsAG , CM000664.2:g.47482873_47482874delinsAG	GRCh38
NC_000002.11:g.47710012_47710013delinsAG , CM000664.1:g.47710012_47710013delinsAG	GRCh37
NC_000002.10:g.47563516_47563517delinsAG	NCBI36
NG_007110.2:g.84750_84751delinsAG , LRG_218:g.84750_84751delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+2002_2634+2003delinsAG	ENSP00000495641.2:n.2634+2002_2634+2003delinsAG
ENST00000233146.7:c.2729_2730delinsAG MANE Select	ENSP00000233146.2:p.Gln910=
ENST00000543555.6:c.2531_2532delinsAG	ENSP00000442697.1:p.Gln844=
ENST00000644092.1:c.*934+2002_*934+2003delinsAG	ENSP00000496351.1:n.*934+2002_*934+2003delinsAG
ENST00000644900.1:c.487+2002_487+2003delinsAG
ENST00000645339.1:c.2634+2002_2634+2003delinsAG	ENSP00000496441.1:n.2634+2002_2634+2003delinsAG
ENST00000645506.1:c.2634+2002_2634+2003delinsAG	ENSP00000495455.1:n.2634+2002_2634+2003delinsAG
ENST00000646415.1:c.2634+2002_2634+2003delinsAG	ENSP00000495543.1:n.2634+2002_2634+2003delinsAG
ENST00000233146.6:c.2729_2730delinsAG	ENSP00000233146.2:p.Gln910=
ENST00000406134.5:c.2634+2002_2634+2003delinsAG	ENSP00000384199.1:n.2634+2002_2634+2003delinsAG
ENST00000461394.5:n.75+2002_75+2003delinsAG
ENST00000543555.5:c.2531_2532delinsAG	ENSP00000442697.1:p.Gln844=
ENST00000610696.4:c.*1125_*1126delinsAG	ENSP00000483159.1:n.*1125_*1126delinsAG
ENST00000613514.4:c.*1269_*1270delinsAG	ENSP00000484137.1:n.*1269_*1270delinsAG
ENST00000617333.3:c.*1495_*1496delinsAG	ENSP00000482468.1:n.*1495_*1496delinsAG
ENST00000617938.4:c.*1701_*1702delinsAG	ENSP00000481158.1:n.*1701_*1702delinsAG
ENST00000621359.2:c.*295_*296delinsAG	ENSP00000481416.1:n.*295_*296delinsAG
NM_000251.2:c.2729_2730delinsAG , LRG_218t1:c.2729_2730delinsAG	NP_000242.1:p.Gln910=
NM_001258281.1:c.2531_2532delinsAG	NP_001245210.1:p.Gln844=
XM_005264332.2:c.2634+2002_2634+2003delinsAG	XP_005264389.2:n.2634+2002_2634+2003delinsAG
XM_011532867.1:c.2634+2002_2634+2003delinsAG	XP_011531169.1:n.2634+2002_2634+2003delinsAG
XR_939685.1:n.2706+2002_2706+2003delinsAG
XM_005264332.4:c.2634+2002_2634+2003delinsAG	XP_005264389.2:n.2634+2002_2634+2003delinsAG
XM_011532867.2:c.2634+2002_2634+2003delinsAG	XP_011531169.1:n.2634+2002_2634+2003delinsAG
XR_001738747.2:n.2696+2002_2696+2003delinsAG
XR_939685.2:n.2696+2002_2696+2003delinsAG
NM_000251.3:c.2729_2730delinsAG MANE Select	NP_000242.1:p.Gln910=