Canonical Allele Identifier: CA349353476
Gene: HOXD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093666T>C , CM000664.2:g.176093666T>C GRCh38
NC_000002.11:g.176958394T>C , CM000664.1:g.176958394T>C GRCh37
NC_000002.10:g.176666640T>C NCBI36
NG_008137.1:g.5863T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.776T>C MANE Select ENSP00000376322.3:p.Phe259Ser
ENST00000392539.3:c.776T>C ENSP00000376322.3:p.Phe259Ser
NM_000523.3:c.776T>C NP_000514.2:p.Phe259Ser
XM_011511068.1:c.725-814T>C XP_011509370.1:n.725-814T>C
XM_011511068.2:c.725-814T>C XP_011509370.1:n.725-814T>C
NM_000523.4:c.776T>C MANE Select NP_000514.2:p.Phe259Ser