Canonical Allele Identifier: CA2495876235

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480967_47480969delinsCTG , CM000664.2:g.47480967_47480969delinsCTG	GRCh38
NC_000002.11:g.47708106_47708108delinsCTG , CM000664.1:g.47708106_47708108delinsCTG	GRCh37
NC_000002.10:g.47561610_47561612delinsCTG	NCBI36
NG_007110.2:g.82844_82846delinsCTG , LRG_218:g.82844_82846delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+96_2634+98delinsCTG	ENSP00000495641.2:n.2634+96_2634+98delinsCTG
ENST00000233146.7:c.2634+96_2634+98delinsCTG MANE Select	ENSP00000233146.2:n.2634+96_2634+98delinsCTG
ENST00000543555.6:c.2436+96_2436+98delinsCTG	ENSP00000442697.1:n.2436+96_2436+98delinsCTG
ENST00000644092.1:c.*934+96_*934+98delinsCTG	ENSP00000496351.1:n.*934+96_*934+98delinsCTG
ENST00000644900.1:c.487+96_487+98delinsCTG
ENST00000645339.1:c.2634+96_2634+98delinsCTG	ENSP00000496441.1:n.2634+96_2634+98delinsCTG
ENST00000645506.1:c.2634+96_2634+98delinsCTG	ENSP00000495455.1:n.2634+96_2634+98delinsCTG
ENST00000646415.1:c.2634+96_2634+98delinsCTG	ENSP00000495543.1:n.2634+96_2634+98delinsCTG
ENST00000233146.6:c.2634+96_2634+98delinsCTG	ENSP00000233146.2:n.2634+96_2634+98delinsCTG
ENST00000406134.5:c.2634+96_2634+98delinsCTG	ENSP00000384199.1:n.2634+96_2634+98delinsCTG
ENST00000461394.5:n.75+96_75+98delinsCTG
ENST00000543555.5:c.2436+96_2436+98delinsCTG	ENSP00000442697.1:n.2436+96_2436+98delinsCTG
ENST00000610696.4:c.*1030+96_*1030+98delinsCTG	ENSP00000483159.1:n.*1030+96_*1030+98delinsCTG
ENST00000613514.4:c.*1174+96_*1174+98delinsCTG	ENSP00000484137.1:n.*1174+96_*1174+98delinsCTG
ENST00000617333.3:c.*1400+96_*1400+98delinsCTG	ENSP00000482468.1:n.*1400+96_*1400+98delinsCTG
ENST00000617938.4:c.*1606+96_*1606+98delinsCTG	ENSP00000481158.1:n.*1606+96_*1606+98delinsCTG
ENST00000621359.2:c.*200+96_*200+98delinsCTG	ENSP00000481416.1:n.*200+96_*200+98delinsCTG
NM_000251.2:c.2634+96_2634+98delinsCTG , LRG_218t1:c.2634+96_2634+98delinsCTG	NP_000242.1:n.2634+96_2634+98delinsCTG
NM_001258281.1:c.2436+96_2436+98delinsCTG	NP_001245210.1:n.2436+96_2436+98delinsCTG
XM_005264332.2:c.2634+96_2634+98delinsCTG	XP_005264389.2:n.2634+96_2634+98delinsCTG
XM_011532867.1:c.2634+96_2634+98delinsCTG	XP_011531169.1:n.2634+96_2634+98delinsCTG
XR_939685.1:n.2706+96_2706+98delinsCTG
XM_005264332.4:c.2634+96_2634+98delinsCTG	XP_005264389.2:n.2634+96_2634+98delinsCTG
XM_011532867.2:c.2634+96_2634+98delinsCTG	XP_011531169.1:n.2634+96_2634+98delinsCTG
XR_001738747.2:n.2696+96_2696+98delinsCTG
XR_939685.2:n.2696+96_2696+98delinsCTG
NM_000251.3:c.2634+96_2634+98delinsCTG MANE Select	NP_000242.1:n.2634+96_2634+98delinsCTG