Canonical Allele Identifier: CA367069689
Gene: HOXA13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198272G>T , CM000669.2:g.27198272G>T GRCh38
NC_000007.13:g.27237891G>T , CM000669.1:g.27237891G>T GRCh37
NC_000007.12:g.27204416G>T NCBI36
NG_008181.1:g.6835C>A
NG_008181.2:g.6835C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1093C>A MANE Select ENSP00000497112.1:p.Gln365Lys
ENST00000222753.5:c.1093C>A ENSP00000222753.4:p.Gln365Lys
NM_000522.4:c.1093C>A NP_000513.2:p.Gln365Lys
XM_011515344.1:c.1093C>A XP_011513646.1:p.Gln365Lys
NM_000522.5:c.1093C>A MANE Select NP_000513.2:p.Gln365Lys