Canonical Allele Identifier: CA4195981
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095695_27095706del , CM000669.2:g.27095695_27095706del GRCh38
NC_000007.13:g.27135314_27135325del , CM000669.1:g.27135314_27135325del GRCh37
NC_000007.12:g.27101839_27101850del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.212_223del MANE Select ENSP00000494260.2:p.His71_His74del
ENST00000343060.4:c.212_223del ENSP00000343246.4:p.His71_His74del
ENST00000355633.5:c.212_223del ENSP00000347851.5:p.His71_His74del
NM_005522.5:c.212_223del MANE Select NP_005513.2:p.His71_His74del
NM_153620.3:c.212_223del NP_705873.3:p.His71_His74del