Canonical Allele Identifier: CA2586964869

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482774_47482776delinsCTT , CM000664.2:g.47482774_47482776delinsCTT	GRCh38
NC_000002.11:g.47709913_47709915delinsCTT , CM000664.1:g.47709913_47709915delinsCTT	GRCh37
NC_000002.10:g.47563417_47563419delinsCTT	NCBI36
NG_007110.2:g.84651_84653delinsCTT , LRG_218:g.84651_84653delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2634+1903_2634+1905delinsCTT	ENSP00000495641.2:n.2634+1903_2634+1905de...
ENST00000233146.7:c.2635-5_2635-3delinsCTT MANE Select	ENSP00000233146.2:n.2635-5_2635-3delinsCT...
ENST00000543555.6:c.2437-5_2437-3delinsCTT	ENSP00000442697.1:n.2437-5_2437-3delinsCT...
ENST00000644092.1:c.*934+1903_*934+1905delinsCTT	ENSP00000496351.1:n.*934+1903_*934+1905de...
ENST00000644900.1:c.487+1903_487+1905delinsCTT
ENST00000645339.1:c.2634+1903_2634+1905delinsCTT	ENSP00000496441.1:n.2634+1903_2634+1905de...
ENST00000645506.1:c.2634+1903_2634+1905delinsCTT	ENSP00000495455.1:n.2634+1903_2634+1905de...
ENST00000646415.1:c.2634+1903_2634+1905delinsCTT	ENSP00000495543.1:n.2634+1903_2634+1905de...
ENST00000233146.6:c.2635-5_2635-3delinsCTT	ENSP00000233146.2:n.2635-5_2635-3delinsCT...
ENST00000406134.5:c.2634+1903_2634+1905delinsCTT	ENSP00000384199.1:n.2634+1903_2634+1905de...
ENST00000461394.5:n.75+1903_75+1905delinsCTT
ENST00000543555.5:c.2437-5_2437-3delinsCTT	ENSP00000442697.1:n.2437-5_2437-3delinsCT...
ENST00000610696.4:c.*1031-5_*1031-3delinsCTT	ENSP00000483159.1:n.*1031-5_*1031-3delins...
ENST00000613514.4:c.*1175-5_*1175-3delinsCTT	ENSP00000484137.1:n.*1175-5_*1175-3delins...
ENST00000617333.3:c.*1401-5_*1401-3delinsCTT	ENSP00000482468.1:n.*1401-5_*1401-3delins...
ENST00000617938.4:c.*1607-5_*1607-3delinsCTT	ENSP00000481158.1:n.*1607-5_*1607-3delins...
ENST00000621359.2:c.*201-5_*201-3delinsCTT	ENSP00000481416.1:n.*201-5_*201-3delinsCT...
NM_000251.2:c.2635-5_2635-3delinsCTT , LRG_218t1:c.2635-5_2635-3delinsCTT	NP_000242.1:n.2635-5_2635-3delinsCTT
NM_001258281.1:c.2437-5_2437-3delinsCTT	NP_001245210.1:n.2437-5_2437-3delinsCTT
XM_005264332.2:c.2634+1903_2634+1905delinsCTT	XP_005264389.2:n.2634+1903_2634+1905delin...
XM_011532867.1:c.2634+1903_2634+1905delinsCTT	XP_011531169.1:n.2634+1903_2634+1905delin...
XR_939685.1:n.2706+1903_2706+1905delinsCTT
XM_005264332.4:c.2634+1903_2634+1905delinsCTT	XP_005264389.2:n.2634+1903_2634+1905delin...
XM_011532867.2:c.2634+1903_2634+1905delinsCTT	XP_011531169.1:n.2634+1903_2634+1905delin...
XR_001738747.2:n.2696+1903_2696+1905delinsCTT
XR_939685.2:n.2696+1903_2696+1905delinsCTT
NM_000251.3:c.2635-5_2635-3delinsCTT MANE Select	NP_000242.1:n.2635-5_2635-3delinsCTT