Canonical Allele Identifier: CA367069513
Gene: HOXA13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198198T>G , CM000669.2:g.27198198T>G GRCh38
NC_000007.13:g.27237817T>G , CM000669.1:g.27237817T>G GRCh37
NC_000007.12:g.27204342T>G NCBI36
NG_008181.1:g.6909A>C
NG_008181.2:g.6909A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.1167A>C MANE Select ENSP00000497112.1:p.Ter389Tyr
ENST00000222753.5:c.1167A>C ENSP00000222753.4:p.Ter389Tyr
NM_000522.4:c.1167A>C NP_000513.2:p.Ter389Tyr
XM_011515344.1:c.1167A>C XP_011513646.1:p.Ter389Tyr
NM_000522.5:c.1167A>C MANE Select NP_000513.2:p.Ter389Tyr