Canonical Allele Identifier: CA2495832562
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47412258_47412263delinsAAAGTG , CM000664.2:g.47412258_47412263delinsAAAGTG GRCh38
NC_000002.11:g.47639397_47639402delinsAAAGTG , CM000664.1:g.47639397_47639402delinsAAAGTG GRCh37
NC_000002.10:g.47492901_47492906delinsAAAGTG NCBI36
NG_007110.2:g.14135_14140delinsAAAGTG , LRG_218:g.14135_14140delinsAAAGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.646-156_646-151delinsAAAGTG ENSP00000495641.2:n.646-156_646-151delinsAAAGTG
ENST00000233146.7:c.646-156_646-151delinsAAAGTG MANE Select ENSP00000233146.2:n.646-156_646-151delinsAAAGTG
ENST00000543555.6:c.448-156_448-151delinsAAAGTG ENSP00000442697.1:n.448-156_448-151delinsAAAGTG
ENST00000644092.1:c.646-156_646-151delinsAAAGTG ENSP00000496351.1:n.646-156_646-151delinsAAAGTG
ENST00000645339.1:c.646-156_646-151delinsAAAGTG ENSP00000496441.1:n.646-156_646-151delinsAAAGTG
ENST00000645506.1:c.646-156_646-151delinsAAAGTG ENSP00000495455.1:n.646-156_646-151delinsAAAGTG
ENST00000646415.1:c.646-156_646-151delinsAAAGTG ENSP00000495543.1:n.646-156_646-151delinsAAAGTG
ENST00000233146.6:c.646-156_646-151delinsAAAGTG ENSP00000233146.2:n.646-156_646-151delinsAAAGTG
ENST00000406134.5:c.646-156_646-151delinsAAAGTG ENSP00000384199.1:n.646-156_646-151delinsAAAGTG
ENST00000543555.5:c.448-156_448-151delinsAAAGTG ENSP00000442697.1:n.448-156_448-151delinsAAAGTG
ENST00000610696.4:c.646-156_646-151delinsAAAGTG ENSP00000483159.1:n.646-156_646-151delinsAAAGTG
ENST00000613514.4:c.646-156_646-151delinsAAAGTG ENSP00000484137.1:n.646-156_646-151delinsAAAGTG
ENST00000617333.3:c.646-156_646-151delinsAAAGTG ENSP00000482468.1:n.646-156_646-151delinsAAAGTG
ENST00000617938.4:c.646-156_646-151delinsAAAGTG ENSP00000481158.1:n.646-156_646-151delinsAAAGTG
ENST00000621359.2:c.646-156_646-151delinsAAAGTG ENSP00000481416.1:n.646-156_646-151delinsAAAGTG
NM_000251.2:c.646-156_646-151delinsAAAGTG , LRG_218t1:c.646-156_646-151delinsAAAGTG NP_000242.1:n.646-156_646-151delinsAAAGTG
NM_001258281.1:c.448-156_448-151delinsAAAGTG NP_001245210.1:n.448-156_448-151delinsAAAGTG
XM_005264332.2:c.646-156_646-151delinsAAAGTG XP_005264389.2:n.646-156_646-151delinsAAAGTG
XM_011532867.1:c.646-156_646-151delinsAAAGTG XP_011531169.1:n.646-156_646-151delinsAAAGTG
XR_939685.1:n.718-156_718-151delinsAAAGTG
XM_005264332.4:c.646-156_646-151delinsAAAGTG XP_005264389.2:n.646-156_646-151delinsAAAGTG
XM_011532867.2:c.646-156_646-151delinsAAAGTG XP_011531169.1:n.646-156_646-151delinsAAAGTG
XR_001738747.2:n.708-156_708-151delinsAAAGTG
XR_939685.2:n.708-156_708-151delinsAAAGTG
NM_000251.3:c.646-156_646-151delinsAAAGTG MANE Select NP_000242.1:n.646-156_646-151delinsAAAGTG