Canonical Allele Identifier: CA1696262935
Gene: HOXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198068A= , CM000669.2:g.27198068A= GRCh38
NC_000007.13:g.27237687A= , CM000669.1:g.27237687A= GRCh37
NC_000007.12:g.27204212A= NCBI36
NG_008181.1:g.7039T=
NG_008181.2:g.7039T=

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*130T= MANE Select ENSP00000497112.1:n.*130T=
ENST00000222753.5:c.*130T= ENSP00000222753.4:n.*130T=
NM_000522.4:c.*130T= NP_000513.2:n.*130T=
XM_011515344.1:c.*130T= XP_011513646.1:n.*130T=
NM_000522.5:c.*130T= MANE Select NP_000513.2:n.*130T=