Canonical Allele Identifier: CA367069679
Gene: HOXA13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198269C>A , CM000669.2:g.27198269C>A GRCh38
NC_000007.13:g.27237888C>A , CM000669.1:g.27237888C>A GRCh37
NC_000007.12:g.27204413C>A NCBI36
NG_008181.1:g.6838G>T
NG_008181.2:g.6838G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1096G>T MANE Select ENSP00000497112.1:p.Val366Phe
ENST00000222753.5:c.1096G>T ENSP00000222753.4:p.Val366Phe
NM_000522.4:c.1096G>T NP_000513.2:p.Val366Phe
XM_011515344.1:c.1096G>T XP_011513646.1:p.Val366Phe
NM_000522.5:c.1096G>T MANE Select NP_000513.2:p.Val366Phe