Canonical Allele Identifier: CA367068650
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095512T>A , CM000669.2:g.27095512T>A GRCh38
NC_000007.13:g.27135131T>A , CM000669.1:g.27135131T>A GRCh37
NC_000007.12:g.27101656T>A NCBI36
NG_011813.1:g.5495A>T
NG_033087.1:g.4419T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.401A>T MANE Select ENSP00000494260.2:p.Asn134Ile
ENST00000343060.4:c.401A>T ENSP00000343246.4:p.Asn134Ile
ENST00000355633.5:c.354+47A>T ENSP00000347851.5:n.354+47A>T
NM_005522.4:c.401A>T NP_005513.1:p.Asn134Ile
NM_153620.2:c.354+47A>T NP_705873.2:n.354+47A>T
NM_005522.5:c.401A>T MANE Select NP_005513.2:p.Asn134Ile
NM_153620.3:c.354+47A>T NP_705873.3:n.354+47A>T