Canonical Allele Identifier: CA2658949595
Gene: MSH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47480952_47480961del , CM000664.2:g.47480952_47480961del GRCh38
NC_000002.11:g.47708091_47708100del , CM000664.1:g.47708091_47708100del GRCh37
NC_000002.10:g.47561595_47561604del NCBI36
NG_007110.2:g.82829_82838del , LRG_218:g.82829_82838del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.2634+81_2634+90del ENSP00000495641.2:n.2634+81_2634+90del
ENST00000233146.7:c.2634+81_2634+90del MANE Select ENSP00000233146.2:n.2634+81_2634+90del
ENST00000543555.6:c.2436+81_2436+90del ENSP00000442697.1:n.2436+81_2436+90del
ENST00000644092.1:c.*934+81_*934+90del ENSP00000496351.1:n.*934+81_*934+90del
ENST00000644900.1:c.487+81_487+90del
ENST00000645339.1:c.2634+81_2634+90del ENSP00000496441.1:n.2634+81_2634+90del
ENST00000645506.1:c.2634+81_2634+90del ENSP00000495455.1:n.2634+81_2634+90del
ENST00000646415.1:c.2634+81_2634+90del ENSP00000495543.1:n.2634+81_2634+90del
ENST00000233146.6:c.2634+81_2634+90del ENSP00000233146.2:n.2634+81_2634+90del
ENST00000406134.5:c.2634+81_2634+90del ENSP00000384199.1:n.2634+81_2634+90del
ENST00000461394.5:n.75+81_75+90del
ENST00000543555.5:c.2436+81_2436+90del ENSP00000442697.1:n.2436+81_2436+90del
ENST00000610696.4:c.*1030+81_*1030+90del ENSP00000483159.1:n.*1030+81_*1030+90del
ENST00000613514.4:c.*1174+81_*1174+90del ENSP00000484137.1:n.*1174+81_*1174+90del
ENST00000617333.3:c.*1400+81_*1400+90del ENSP00000482468.1:n.*1400+81_*1400+90del
ENST00000617938.4:c.*1606+81_*1606+90del ENSP00000481158.1:n.*1606+81_*1606+90del
ENST00000621359.2:c.*200+81_*200+90del ENSP00000481416.1:n.*200+81_*200+90del
NM_000251.2:c.2634+81_2634+90del , LRG_218t1:c.2634+81_2634+90del NP_000242.1:n.2634+81_2634+90del
NM_001258281.1:c.2436+81_2436+90del NP_001245210.1:n.2436+81_2436+90del
XM_005264332.2:c.2634+81_2634+90del XP_005264389.2:n.2634+81_2634+90del
XM_011532867.1:c.2634+81_2634+90del XP_011531169.1:n.2634+81_2634+90del
XR_939685.1:n.2706+81_2706+90del
XM_005264332.4:c.2634+81_2634+90del XP_005264389.2:n.2634+81_2634+90del
XM_011532867.2:c.2634+81_2634+90del XP_011531169.1:n.2634+81_2634+90del
XR_001738747.2:n.2696+81_2696+90del
XR_939685.2:n.2696+81_2696+90del
NM_000251.3:c.2634+81_2634+90del MANE Select NP_000242.1:n.2634+81_2634+90del