Canonical Allele Identifier: CA1696262955
Gene: HOXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198077T= , CM000669.2:g.27198077T= GRCh38
NC_000007.13:g.27237696T= , CM000669.1:g.27237696T= GRCh37
NC_000007.12:g.27204221T= NCBI36
NG_008181.1:g.7030A=
NG_008181.2:g.7030A=

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*121A= MANE Select ENSP00000497112.1:n.*121A=
ENST00000222753.5:c.*121A= ENSP00000222753.4:n.*121A=
NM_000522.4:c.*121A= NP_000513.2:n.*121A=
XM_011515344.1:c.*121A= XP_011513646.1:n.*121A=
NM_000522.5:c.*121A= MANE Select NP_000513.2:n.*121A=