Canonical Allele Identifier: CA2495872425

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475074T= , CM000664.2:g.47475074T=	GRCh38
NC_000002.11:g.47702213T= , CM000664.1:g.47702213T=	GRCh37
NC_000002.10:g.47555717T=	NCBI36
NG_007110.2:g.76951T= , LRG_218:g.76951T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1809T=	ENSP00000495641.2:p.Asp603=
ENST00000233146.7:c.1809T= MANE Select	ENSP00000233146.2:p.Asp603=
ENST00000543555.6:c.1611T=	ENSP00000442697.1:p.Asp537=
ENST00000644092.1:c.*109T=	ENSP00000496351.1:n.*109T=
ENST00000645339.1:c.1809T=	ENSP00000496441.1:p.Asp603=
ENST00000645506.1:c.1809T=	ENSP00000495455.1:p.Asp603=
ENST00000646415.1:c.1809T=	ENSP00000495543.1:p.Asp603=
ENST00000233146.6:c.1809T=	ENSP00000233146.2:p.Asp603=
ENST00000406134.5:c.1809T=	ENSP00000384199.1:p.Asp603=
ENST00000543555.5:c.1611T=	ENSP00000442697.1:p.Asp537=
ENST00000610696.4:c.*205T=	ENSP00000483159.1:n.*205T=
ENST00000613514.4:c.*349T=	ENSP00000484137.1:n.*349T=
ENST00000617333.3:c.*575T=	ENSP00000482468.1:n.*575T=
ENST00000617938.4:c.*781T=	ENSP00000481158.1:n.*781T=
ENST00000621359.2:c.1809T=	ENSP00000481416.1:p.Asp603=
NM_000251.2:c.1809T= , LRG_218t1:c.1809T=	NP_000242.1:p.Asp603=
NM_001258281.1:c.1611T=	NP_001245210.1:p.Asp537=
XM_005264332.2:c.1809T=	XP_005264389.2:p.Asp603=
XM_011532867.1:c.1809T=	XP_011531169.1:p.Asp603=
XR_939685.1:n.1881T=
XM_005264332.4:c.1809T=	XP_005264389.2:p.Asp603=
XM_011532867.2:c.1809T=	XP_011531169.1:p.Asp603=
XR_001738747.2:n.1871T=
XR_939685.2:n.1871T=
NM_000251.3:c.1809T= MANE Select	NP_000242.1:p.Asp603=