Canonical Allele Identifier: CA2573139916
Gene: MSH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873117_80873118delinsTA , CM000667.2:g.80873117_80873118delinsTA GRCh38
NC_000005.9:g.80168936_80168937delinsTA , CM000667.1:g.80168936_80168937delinsTA GRCh37
NC_000005.8:g.80204692_80204693delinsTA NCBI36
NG_016607.1:g.223643_223644delinsTA
NG_016607.2:g.223643_223644delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3132_3133delinsTA MANE Select ENSP00000265081.6:p.Ala1045Thr
ENST00000658259.1:c.2964_2965delinsTA ENSP00000499617.1:p.Ala989Thr
ENST00000659302.1:c.540_541delinsTA
ENST00000667069.1:c.2937_2938delinsTA ENSP00000499502.1:p.Ala980Thr
ENST00000670357.1:c.*456_*457delinsTA ENSP00000499791.1:n.*456_*457delinsTA
ENST00000265081.6:c.3132_3133delinsTA ENSP00000265081.6:p.Ala1045Thr
NM_002439.4:c.3132_3133delinsTA NP_002430.3:p.Ala1045Thr
NM_002439.5:c.3132_3133delinsTA MANE Select NP_002430.3:p.Ala1045Thr
Search 100 bp 5'
Search 100 bp 3'