Canonical Allele Identifier: CA658760710

Gene: MSH2

Linked Data

• PubMed: PMID:75

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47411348_47413406del , CM000664.2:g.47411348_47413406del	GRCh38
NC_000002.11:g.47638487_47640545del , CM000664.1:g.47638487_47640545del	GRCh37
NC_000002.10:g.47491991_47494049del	NCBI36
NG_007110.2:g.13225_15283del , LRG_218:g.13225_15283del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.645+976_792+846del
ENST00000233146.7:c.645+976_792+846del
ENST00000543555.6:c.447+976_594+846del
ENST00000644092.1:c.645+976_792+846del
ENST00000645339.1:c.645+976_792+846del
ENST00000645506.1:c.645+976_792+846del
ENST00000646415.1:c.645+976_792+846del
ENST00000233146.6:c.645+976_792+846del
ENST00000406134.5:c.645+976_792+846del
ENST00000543555.5:c.447+976_594+846del
ENST00000610696.4:c.645+976_792+846del
ENST00000613514.4:c.645+976_792+846del
ENST00000617333.3:c.645+976_792+846del
ENST00000617938.4:c.645+976_792+846del
ENST00000621359.2:c.645+976_792+846del
NM_000251.2:c.645+976_792+846del , LRG_218t1:c.645+976_792+846del
NM_001258281.1:c.447+976_594+846del
XM_005264332.2:c.645+976_792+846del
XM_011532867.1:c.645+976_792+846del
XR_939685.1:n.717+976_864+846del
XM_005264332.4:c.645+976_792+846del
XM_011532867.2:c.645+976_792+846del
XR_001738747.2:n.707+976_854+846del
XR_939685.2:n.707+976_854+846del
NM_000251.3:c.645+976_792+846del