Canonical Allele Identifier: CA367069032
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095653C>A , CM000669.2:g.27095653C>A GRCh38
NC_000007.13:g.27135272C>A , CM000669.1:g.27135272C>A GRCh37
NC_000007.12:g.27101797C>A NCBI36
NG_011813.1:g.5354G>T
NG_033087.1:g.4560C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.260G>T MANE Select ENSP00000494260.2:p.Gly87Val
ENST00000343060.4:c.260G>T ENSP00000343246.4:p.Gly87Val
ENST00000355633.5:c.260G>T ENSP00000347851.5:p.Gly87Val
NM_005522.4:c.260G>T NP_005513.1:p.Gly87Val
NM_153620.2:c.260G>T NP_705873.2:p.Gly87Val
NM_005522.5:c.260G>T MANE Select NP_005513.2:p.Gly87Val
NM_153620.3:c.260G>T NP_705873.3:p.Gly87Val