Canonical Allele Identifier: CA2495832769
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47412530_47412534delinsTAGTG , CM000664.2:g.47412530_47412534delinsTAGTG GRCh38
NC_000002.11:g.47639669_47639673delinsTAGTG , CM000664.1:g.47639669_47639673delinsTAGTG GRCh37
NC_000002.10:g.47493173_47493177delinsTAGTG NCBI36
NG_007110.2:g.14407_14411delinsTAGTG , LRG_218:g.14407_14411delinsTAGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.762_766delinsTAGTG ENSP00000495641.2:p.Asn254=
ENST00000233146.7:c.762_766delinsTAGTG MANE Select ENSP00000233146.2:p.Asn254=
ENST00000543555.6:c.564_568delinsTAGTG ENSP00000442697.1:p.Asn188=
ENST00000644092.1:c.762_766delinsTAGTG ENSP00000496351.1:p.Asn254=
ENST00000645339.1:c.762_766delinsTAGTG ENSP00000496441.1:p.Asn254=
ENST00000645506.1:c.762_766delinsTAGTG ENSP00000495455.1:p.Asn254=
ENST00000646415.1:c.762_766delinsTAGTG ENSP00000495543.1:p.Asn254=
ENST00000233146.6:c.762_766delinsTAGTG ENSP00000233146.2:p.Asn254=
ENST00000406134.5:c.762_766delinsTAGTG ENSP00000384199.1:p.Asn254=
ENST00000543555.5:c.564_568delinsTAGTG ENSP00000442697.1:p.Asn188=
ENST00000610696.4:c.762_766delinsTAGTG ENSP00000483159.1:p.Asn254=
ENST00000613514.4:c.762_766delinsTAGTG ENSP00000484137.1:p.Asn254=
ENST00000617333.3:c.762_766delinsTAGTG ENSP00000482468.1:p.Asn254=
ENST00000617938.4:c.762_766delinsTAGTG ENSP00000481158.1:p.Asn254=
ENST00000621359.2:c.762_766delinsTAGTG ENSP00000481416.1:p.Asn254=
NM_000251.2:c.762_766delinsTAGTG , LRG_218t1:c.762_766delinsTAGTG NP_000242.1:p.Asn254=
NM_001258281.1:c.564_568delinsTAGTG NP_001245210.1:p.Asn188=
XM_005264332.2:c.762_766delinsTAGTG XP_005264389.2:p.Asn254=
XM_011532867.1:c.762_766delinsTAGTG XP_011531169.1:p.Asn254=
XR_939685.1:n.834_838delinsTAGTG
XM_005264332.4:c.762_766delinsTAGTG XP_005264389.2:p.Asn254=
XM_011532867.2:c.762_766delinsTAGTG XP_011531169.1:p.Asn254=
XR_001738747.2:n.824_828delinsTAGTG
XR_939685.2:n.824_828delinsTAGTG
NM_000251.3:c.762_766delinsTAGTG MANE Select NP_000242.1:p.Asn254=