Canonical Allele Identifier: CA1696186886
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095435T= , CM000669.2:g.27095435T= GRCh38
NC_000007.13:g.27135054T= , CM000669.1:g.27135054T= GRCh37
NC_000007.12:g.27101579T= NCBI36
NG_011813.1:g.5572A=
NG_033087.1:g.4342T=

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.478A= MANE Select ENSP00000494260.2:p.Ile160=
ENST00000343060.4:c.478A= ENSP00000343246.4:p.Ile160=
ENST00000355633.5:c.355-80A= ENSP00000347851.5:n.355-80A=
NM_005522.4:c.478A= NP_005513.1:p.Ile160=
NM_153620.2:c.355-80A= NP_705873.2:n.355-80A=
NM_005522.5:c.478A= MANE Select NP_005513.2:p.Ile160=
NM_153620.3:c.355-80A= NP_705873.3:n.355-80A=