Canonical Allele Identifier: CA2495832832
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47412611_47412616delinsTATATA , CM000664.2:g.47412611_47412616delinsTATATA GRCh38
NC_000002.11:g.47639750_47639755delinsTATATA , CM000664.1:g.47639750_47639755delinsTATATA GRCh37
NC_000002.10:g.47493254_47493259delinsTATATA NCBI36
NG_007110.2:g.14488_14493delinsTATATA , LRG_218:g.14488_14493delinsTATATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.792+51_792+56delinsTATATA ENSP00000495641.2:n.792+51_792+56delinsTATATA
ENST00000233146.7:c.792+51_792+56delinsTATATA MANE Select ENSP00000233146.2:n.792+51_792+56delinsTATATA
ENST00000543555.6:c.594+51_594+56delinsTATATA ENSP00000442697.1:n.594+51_594+56delinsTATATA
ENST00000644092.1:c.792+51_792+56delinsTATATA ENSP00000496351.1:n.792+51_792+56delinsTATATA
ENST00000645339.1:c.792+51_792+56delinsTATATA ENSP00000496441.1:n.792+51_792+56delinsTATATA
ENST00000645506.1:c.792+51_792+56delinsTATATA ENSP00000495455.1:n.792+51_792+56delinsTATATA
ENST00000646415.1:c.792+51_792+56delinsTATATA ENSP00000495543.1:n.792+51_792+56delinsTATATA
ENST00000233146.6:c.792+51_792+56delinsTATATA ENSP00000233146.2:n.792+51_792+56delinsTATATA
ENST00000406134.5:c.792+51_792+56delinsTATATA ENSP00000384199.1:n.792+51_792+56delinsTATATA
ENST00000543555.5:c.594+51_594+56delinsTATATA ENSP00000442697.1:n.594+51_594+56delinsTATATA
ENST00000610696.4:c.792+51_792+56delinsTATATA ENSP00000483159.1:n.792+51_792+56delinsTATATA
ENST00000613514.4:c.792+51_792+56delinsTATATA ENSP00000484137.1:n.792+51_792+56delinsTATATA
ENST00000617333.3:c.792+51_792+56delinsTATATA ENSP00000482468.1:n.792+51_792+56delinsTATATA
ENST00000617938.4:c.792+51_792+56delinsTATATA ENSP00000481158.1:n.792+51_792+56delinsTATATA
ENST00000621359.2:c.792+51_792+56delinsTATATA ENSP00000481416.1:n.792+51_792+56delinsTATATA
NM_000251.2:c.792+51_792+56delinsTATATA , LRG_218t1:c.792+51_792+56delinsTATATA NP_000242.1:n.792+51_792+56delinsTATATA
NM_001258281.1:c.594+51_594+56delinsTATATA NP_001245210.1:n.594+51_594+56delinsTATATA
XM_005264332.2:c.792+51_792+56delinsTATATA XP_005264389.2:n.792+51_792+56delinsTATATA
XM_011532867.1:c.792+51_792+56delinsTATATA XP_011531169.1:n.792+51_792+56delinsTATATA
XR_939685.1:n.864+51_864+56delinsTATATA
XM_005264332.4:c.792+51_792+56delinsTATATA XP_005264389.2:n.792+51_792+56delinsTATATA
XM_011532867.2:c.792+51_792+56delinsTATATA XP_011531169.1:n.792+51_792+56delinsTATATA
XR_001738747.2:n.854+51_854+56delinsTATATA
XR_939685.2:n.854+51_854+56delinsTATATA
NM_000251.3:c.792+51_792+56delinsTATATA MANE Select NP_000242.1:n.792+51_792+56delinsTATATA