Canonical Allele Identifier: CA1696262932
Gene: HOXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198063G= , CM000669.2:g.27198063G= GRCh38
NC_000007.13:g.27237682G= , CM000669.1:g.27237682G= GRCh37
NC_000007.12:g.27204207G= NCBI36
NG_008181.1:g.7044C=
NG_008181.2:g.7044C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*135C= MANE Select ENSP00000497112.1:n.*135C=
ENST00000222753.5:c.*135C= ENSP00000222753.4:n.*135C=
NM_000522.4:c.*135C= NP_000513.2:n.*135C=
XM_011515344.1:c.*135C= XP_011513646.1:n.*135C=
NM_000522.5:c.*135C= MANE Select NP_000513.2:n.*135C=