Canonical Allele Identifier: CA2495832693

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412446_47412448delinsAAG , CM000664.2:g.47412446_47412448delinsAAG	GRCh38
NC_000002.11:g.47639585_47639587delinsAAG , CM000664.1:g.47639585_47639587delinsAAG	GRCh37
NC_000002.10:g.47493089_47493091delinsAAG	NCBI36
NG_007110.2:g.14323_14325delinsAAG , LRG_218:g.14323_14325delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.678_680delinsAAG	ENSP00000495641.2:p.Glu226=
ENST00000233146.7:c.678_680delinsAAG MANE Select	ENSP00000233146.2:p.Glu226=
ENST00000543555.6:c.480_482delinsAAG	ENSP00000442697.1:p.Glu160=
ENST00000644092.1:c.678_680delinsAAG	ENSP00000496351.1:p.Glu226=
ENST00000645339.1:c.678_680delinsAAG	ENSP00000496441.1:p.Glu226=
ENST00000645506.1:c.678_680delinsAAG	ENSP00000495455.1:p.Glu226=
ENST00000646415.1:c.678_680delinsAAG	ENSP00000495543.1:p.Glu226=
ENST00000233146.6:c.678_680delinsAAG	ENSP00000233146.2:p.Glu226=
ENST00000406134.5:c.678_680delinsAAG	ENSP00000384199.1:p.Glu226=
ENST00000543555.5:c.480_482delinsAAG	ENSP00000442697.1:p.Glu160=
ENST00000610696.4:c.678_680delinsAAG	ENSP00000483159.1:p.Glu226=
ENST00000613514.4:c.678_680delinsAAG	ENSP00000484137.1:p.Glu226=
ENST00000617333.3:c.678_680delinsAAG	ENSP00000482468.1:p.Glu226=
ENST00000617938.4:c.678_680delinsAAG	ENSP00000481158.1:p.Glu226=
ENST00000621359.2:c.678_680delinsAAG	ENSP00000481416.1:p.Glu226=
NM_000251.2:c.678_680delinsAAG , LRG_218t1:c.678_680delinsAAG	NP_000242.1:p.Glu226=
NM_001258281.1:c.480_482delinsAAG	NP_001245210.1:p.Glu160=
XM_005264332.2:c.678_680delinsAAG	XP_005264389.2:p.Glu226=
XM_011532867.1:c.678_680delinsAAG	XP_011531169.1:p.Glu226=
XR_939685.1:n.750_752delinsAAG
XM_005264332.4:c.678_680delinsAAG	XP_005264389.2:p.Glu226=
XM_011532867.2:c.678_680delinsAAG	XP_011531169.1:p.Glu226=
XR_001738747.2:n.740_742delinsAAG
XR_939685.2:n.740_742delinsAAG
NM_000251.3:c.678_680delinsAAG MANE Select	NP_000242.1:p.Glu226=