Canonical Allele Identifier: CA1696187286
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095698T= , CM000669.2:g.27095698T= GRCh38
NC_000007.13:g.27135317T= , CM000669.1:g.27135317T= GRCh37
NC_000007.12:g.27101842T= NCBI36
NG_011813.1:g.5309A=
NG_033087.1:g.4605T=

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.215A= MANE Select ENSP00000494260.2:p.His72=
ENST00000343060.4:c.215A= ENSP00000343246.4:p.His72=
ENST00000355633.5:c.215A= ENSP00000347851.5:p.His72=
NM_005522.4:c.215A= NP_005513.1:p.His72=
NM_153620.2:c.215A= NP_705873.2:p.His72=
NM_005522.5:c.215A= MANE Select NP_005513.2:p.His72=
NM_153620.3:c.215A= NP_705873.3:p.His72=