Canonical Allele Identifier: CA4195991

Gene: HOXA1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095694_27095695insTGA , CM000669.2:g.27095694_27095695insTGA	GRCh38
NC_000007.13:g.27135313_27135314insTGA , CM000669.1:g.27135313_27135314insTGA	GRCh37
NC_000007.12:g.27101838_27101839insTGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.218_219insTCA MANE Select	ENSP00000494260.2:p.Arg73_His74insHis
ENST00000343060.4:c.218_219insTCA	ENSP00000343246.4:p.Arg73_His74insHis
ENST00000355633.5:c.218_219insTCA	ENSP00000347851.5:p.Arg73_His74insHis
NM_005522.5:c.218_219insTCA MANE Select	NP_005513.2:p.Arg73_His74insHis
NM_153620.3:c.218_219insTCA	NP_705873.3:p.Arg73_His74insHis