Canonical Allele Identifier: CA1696263361
Gene: HOXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198275G= , CM000669.2:g.27198275G= GRCh38
NC_000007.13:g.27237894G= , CM000669.1:g.27237894G= GRCh37
NC_000007.12:g.27204419G= NCBI36
NG_008181.1:g.6832C=
NG_008181.2:g.6832C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.1090C= MANE Select ENSP00000497112.1:p.Arg364=
ENST00000222753.5:c.1090C= ENSP00000222753.4:p.Arg364=
NM_000522.4:c.1090C= NP_000513.2:p.Arg364=
XM_011515344.1:c.1090C= XP_011513646.1:p.Arg364=
NM_000522.5:c.1090C= MANE Select NP_000513.2:p.Arg364=