Canonical Allele Identifier: CA1696263107
Gene: HOXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198173G= , CM000669.2:g.27198173G= GRCh38
NC_000007.13:g.27237792G= , CM000669.1:g.27237792G= GRCh37
NC_000007.12:g.27204317G= NCBI36
NG_008181.1:g.6934C=
NG_008181.2:g.6934C=

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*25C= MANE Select ENSP00000497112.1:n.*25C=
ENST00000222753.5:c.*25C= ENSP00000222753.4:n.*25C=
NM_000522.4:c.*25C= NP_000513.2:n.*25C=
XM_011515344.1:c.*25C= XP_011513646.1:n.*25C=
NM_000522.5:c.*25C= MANE Select NP_000513.2:n.*25C=