Canonical Allele Identifier: CA1696263168
Gene: HOXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198194T= , CM000669.2:g.27198194T= GRCh38
NC_000007.13:g.27237813T= , CM000669.1:g.27237813T= GRCh37
NC_000007.12:g.27204338T= NCBI36
NG_008181.1:g.6913A=
NG_008181.2:g.6913A=

Transcript Alleles

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