Canonical Allele Identifier: CA4195998

Gene: HOXA1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095716_27095721del , CM000669.2:g.27095716_27095721del	GRCh38
NC_000007.13:g.27135335_27135340del , CM000669.1:g.27135335_27135340del	GRCh37
NC_000007.12:g.27101860_27101865del	NCBI36
NG_011813.1:g.5304_5309del
NG_033087.1:g.4623_4628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.210_215del MANE Select	ENSP00000494260.2:p.His71_His72del
ENST00000343060.4:c.210_215del	ENSP00000343246.4:p.His71_His72del
ENST00000355633.5:c.210_215del	ENSP00000347851.5:p.His71_His72del
NM_005522.4:c.210_215del	NP_005513.1:p.His71_His72del
NM_153620.2:c.210_215del	NP_705873.2:p.His71_His72del
NM_005522.5:c.210_215del MANE Select	NP_005513.2:p.His71_His72del
NM_153620.3:c.210_215del	NP_705873.3:p.His71_His72del