Canonical Allele Identifier: CA2658949655

Gene: MSH2

Linked Data

• gnomAD v4: 2-47482666-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482667_47482668del , CM000664.2:g.47482667_47482668del	GRCh38
NC_000002.11:g.47709806_47709807del , CM000664.1:g.47709806_47709807del	GRCh37
NC_000002.10:g.47563310_47563311del	NCBI36
NG_007110.2:g.84544_84545del , LRG_218:g.84544_84545del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+1796_2634+1797del	ENSP00000495641.2:n.2634+1796_2634+1797del
ENST00000233146.7:c.2635-112_2635-111del MANE Select	ENSP00000233146.2:n.2635-112_2635-111del
ENST00000543555.6:c.2437-112_2437-111del	ENSP00000442697.1:n.2437-112_2437-111del
ENST00000644092.1:c.*934+1796_*934+1797del	ENSP00000496351.1:n.*934+1796_*934+1797del
ENST00000644900.1:c.487+1796_487+1797del
ENST00000645339.1:c.2634+1796_2634+1797del	ENSP00000496441.1:n.2634+1796_2634+1797del
ENST00000645506.1:c.2634+1796_2634+1797del	ENSP00000495455.1:n.2634+1796_2634+1797del
ENST00000646415.1:c.2634+1796_2634+1797del	ENSP00000495543.1:n.2634+1796_2634+1797del
ENST00000233146.6:c.2635-112_2635-111del	ENSP00000233146.2:n.2635-112_2635-111del
ENST00000406134.5:c.2634+1796_2634+1797del	ENSP00000384199.1:n.2634+1796_2634+1797del
ENST00000461394.5:n.75+1796_75+1797del
ENST00000543555.5:c.2437-112_2437-111del	ENSP00000442697.1:n.2437-112_2437-111del
ENST00000610696.4:c.*1031-112_*1031-111del	ENSP00000483159.1:n.*1031-112_*1031-111del
ENST00000613514.4:c.*1175-112_*1175-111del	ENSP00000484137.1:n.*1175-112_*1175-111del
ENST00000617333.3:c.*1401-112_*1401-111del	ENSP00000482468.1:n.*1401-112_*1401-111del
ENST00000617938.4:c.*1607-112_*1607-111del	ENSP00000481158.1:n.*1607-112_*1607-111del
ENST00000621359.2:c.*201-112_*201-111del	ENSP00000481416.1:n.*201-112_*201-111del
NM_000251.2:c.2635-112_2635-111del , LRG_218t1:c.2635-112_2635-111del	NP_000242.1:n.2635-112_2635-111del
NM_001258281.1:c.2437-112_2437-111del	NP_001245210.1:n.2437-112_2437-111del
XM_005264332.2:c.2634+1796_2634+1797del	XP_005264389.2:n.2634+1796_2634+1797del
XM_011532867.1:c.2634+1796_2634+1797del	XP_011531169.1:n.2634+1796_2634+1797del
XR_939685.1:n.2706+1796_2706+1797del
XM_005264332.4:c.2634+1796_2634+1797del	XP_005264389.2:n.2634+1796_2634+1797del
XM_011532867.2:c.2634+1796_2634+1797del	XP_011531169.1:n.2634+1796_2634+1797del
XR_001738747.2:n.2696+1796_2696+1797del
XR_939685.2:n.2696+1796_2696+1797del
NM_000251.3:c.2635-112_2635-111del MANE Select	NP_000242.1:n.2635-112_2635-111del