Canonical Allele Identifier: CA367068871
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095603A>T , CM000669.2:g.27095603A>T GRCh38
NC_000007.13:g.27135222A>T , CM000669.1:g.27135222A>T GRCh37
NC_000007.12:g.27101747A>T NCBI36
NG_011813.1:g.5404T>A
NG_033087.1:g.4510A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.310T>A MANE Select ENSP00000494260.2:p.Phe104Ile
ENST00000343060.4:c.310T>A ENSP00000343246.4:p.Phe104Ile
ENST00000355633.5:c.310T>A ENSP00000347851.5:p.Phe104Ile
NM_005522.4:c.310T>A NP_005513.1:p.Phe104Ile
NM_153620.2:c.310T>A NP_705873.2:p.Phe104Ile
NM_005522.5:c.310T>A MANE Select NP_005513.2:p.Phe104Ile
NM_153620.3:c.310T>A NP_705873.3:p.Phe104Ile