Canonical Allele Identifier: CA2682128402
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095604del , CM000669.2:g.27095604del GRCh38
NC_000007.13:g.27135223del , CM000669.1:g.27135223del GRCh37
NC_000007.12:g.27101748del NCBI36
NG_011813.1:g.5403del
NG_033087.1:g.4511del

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.309del MANE Select ENSP00000494260.2:p.Phe104SerfsTer10
ENST00000343060.4:c.309del ENSP00000343246.4:p.Phe104SerfsTer10
ENST00000355633.5:c.309del ENSP00000347851.5:p.Phe104SerfsTer10
NM_005522.4:c.309del NP_005513.1:p.Phe104SerfsTer10
NM_153620.2:c.309del NP_705873.2:p.Phe104SerfsTer10
NM_005522.5:c.309del MANE Select NP_005513.2:p.Phe104SerfsTer10
NM_153620.3:c.309del NP_705873.3:p.Phe104SerfsTer10