Canonical Allele Identifier: CA2695200755

Gene: MSH2

Linked Data

• ClinVar Variation Id: 2673298
• ClinVar RCV Id: RCV003455923

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412409_47412423del , CM000664.2:g.47412409_47412423del	GRCh38
NC_000002.11:g.47639548_47639562del , CM000664.1:g.47639548_47639562del	GRCh37
NC_000002.10:g.47493052_47493066del	NCBI36
NG_007110.2:g.14286_14300del , LRG_218:g.14286_14300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.646-5_655del
ENST00000233146.7:c.646-5_655del
ENST00000543555.6:c.448-5_457del
ENST00000644092.1:c.646-5_655del
ENST00000645339.1:c.646-5_655del
ENST00000645506.1:c.646-5_655del
ENST00000646415.1:c.646-5_655del
ENST00000233146.6:c.646-5_655del
ENST00000406134.5:c.646-5_655del
ENST00000543555.5:c.448-5_457del
ENST00000610696.4:c.646-5_655del
ENST00000613514.4:c.646-5_655del
ENST00000617333.3:c.646-5_655del
ENST00000617938.4:c.646-5_655del
ENST00000621359.2:c.646-5_655del
NM_000251.2:c.646-5_655del , LRG_218t1:c.646-5_655del
NM_001258281.1:c.448-5_457del
XM_005264332.2:c.646-5_655del
XM_011532867.1:c.646-5_655del
XR_939685.1:n.718-5_727del
XM_005264332.4:c.646-5_655del
XM_011532867.2:c.646-5_655del
XR_001738747.2:n.708-5_717del
XR_939685.2:n.708-5_717del
NM_000251.3:c.646-5_655del