Canonical Allele Identifier: CA2495877180

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482615_47482616delinsTG , CM000664.2:g.47482615_47482616delinsTG	GRCh38
NC_000002.11:g.47709754_47709755delinsTG , CM000664.1:g.47709754_47709755delinsTG	GRCh37
NC_000002.10:g.47563258_47563259delinsTG	NCBI36
NG_007110.2:g.84492_84493delinsTG , LRG_218:g.84492_84493delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2634+1744_2634+1745delinsTG	ENSP00000495641.2:n.2634+1744_2634+1745de...
ENST00000233146.7:c.2635-164_2635-163delinsTG MANE Select	ENSP00000233146.2:n.2635-164_2635-163deli...
ENST00000543555.6:c.2437-164_2437-163delinsTG	ENSP00000442697.1:n.2437-164_2437-163deli...
ENST00000644092.1:c.*934+1744_*934+1745delinsTG	ENSP00000496351.1:n.*934+1744_*934+1745de...
ENST00000644900.1:c.487+1744_487+1745delinsTG
ENST00000645339.1:c.2634+1744_2634+1745delinsTG	ENSP00000496441.1:n.2634+1744_2634+1745de...
ENST00000645506.1:c.2634+1744_2634+1745delinsTG	ENSP00000495455.1:n.2634+1744_2634+1745de...
ENST00000646415.1:c.2634+1744_2634+1745delinsTG	ENSP00000495543.1:n.2634+1744_2634+1745de...
ENST00000233146.6:c.2635-164_2635-163delinsTG	ENSP00000233146.2:n.2635-164_2635-163deli...
ENST00000406134.5:c.2634+1744_2634+1745delinsTG	ENSP00000384199.1:n.2634+1744_2634+1745de...
ENST00000461394.5:n.75+1744_75+1745delinsTG
ENST00000543555.5:c.2437-164_2437-163delinsTG	ENSP00000442697.1:n.2437-164_2437-163deli...
ENST00000610696.4:c.*1031-164_*1031-163delinsTG	ENSP00000483159.1:n.*1031-164_*1031-163de...
ENST00000613514.4:c.*1175-164_*1175-163delinsTG	ENSP00000484137.1:n.*1175-164_*1175-163de...
ENST00000617333.3:c.*1401-164_*1401-163delinsTG	ENSP00000482468.1:n.*1401-164_*1401-163de...
ENST00000617938.4:c.*1607-164_*1607-163delinsTG	ENSP00000481158.1:n.*1607-164_*1607-163de...
ENST00000621359.2:c.*201-164_*201-163delinsTG	ENSP00000481416.1:n.*201-164_*201-163deli...
NM_000251.2:c.2635-164_2635-163delinsTG , LRG_218t1:c.2635-164_2635-163delinsTG	NP_000242.1:n.2635-164_2635-163delinsTG
NM_001258281.1:c.2437-164_2437-163delinsTG	NP_001245210.1:n.2437-164_2437-163delinsT...
XM_005264332.2:c.2634+1744_2634+1745delinsTG	XP_005264389.2:n.2634+1744_2634+1745delin...
XM_011532867.1:c.2634+1744_2634+1745delinsTG	XP_011531169.1:n.2634+1744_2634+1745delin...
XR_939685.1:n.2706+1744_2706+1745delinsTG
XM_005264332.4:c.2634+1744_2634+1745delinsTG	XP_005264389.2:n.2634+1744_2634+1745delin...
XM_011532867.2:c.2634+1744_2634+1745delinsTG	XP_011531169.1:n.2634+1744_2634+1745delin...
XR_001738747.2:n.2696+1744_2696+1745delinsTG
XR_939685.2:n.2696+1744_2696+1745delinsTG
NM_000251.3:c.2635-164_2635-163delinsTG MANE Select	NP_000242.1:n.2635-164_2635-163delinsTG