Canonical Allele Identifier: CA1938907813
Gene: HSPA12A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.116816643A= , CM000672.2:g.116816643A= GRCh38
NC_000010.10:g.118576154A= , CM000672.1:g.118576154A= GRCh37
NC_000010.9:g.118566144A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000635765.1:c.91+18292T= ENSP00000489674.1:n.91+18292T=
ENST00000674167.1:c.-124+18292T= ENSP00000501417.1:n.-124+18292T=
ENST00000674197.1:c.88+18292T= ENSP00000501472.1:n.88+18292T=
ENST00000674401.1:c.-210+32923T= ENSP00000501414.1:n.-210+32923T=
ENST00000674505.1:c.-210+32923T= ENSP00000501396.1:n.-210+32923T=
XM_005269672.2:c.91+18292T= XP_005269729.1:n.91+18292T=
XM_005269673.3:c.88+18292T= XP_005269730.1:n.88+18292T=
XM_011539579.1:c.88+18292T= XP_011537881.1:n.88+18292T=
NM_001330164.1:c.91+18292T= NP_001317093.1:n.91+18292T=
XM_005269673.5:c.88+18292T= XP_005269730.1:n.88+18292T=
XM_011539579.2:c.88+18292T= XP_011537881.1:n.88+18292T=
NM_001330164.2:c.91+18292T= NP_001317093.1:n.91+18292T=