Canonical Allele Identifier: CA367068554
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095468A>T , CM000669.2:g.27095468A>T GRCh38
NC_000007.13:g.27135087A>T , CM000669.1:g.27135087A>T GRCh37
NC_000007.12:g.27101612A>T NCBI36
NG_011813.1:g.5539T>A
NG_033087.1:g.4375A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.445T>A MANE Select ENSP00000494260.2:p.Tyr149Asn
ENST00000343060.4:c.445T>A ENSP00000343246.4:p.Tyr149Asn
ENST00000355633.5:c.354+91T>A ENSP00000347851.5:n.354+91T>A
NM_005522.4:c.445T>A NP_005513.1:p.Tyr149Asn
NM_153620.2:c.354+91T>A NP_705873.2:n.354+91T>A
NM_005522.5:c.445T>A MANE Select NP_005513.2:p.Tyr149Asn
NM_153620.3:c.354+91T>A NP_705873.3:n.354+91T>A