Canonical Allele Identifier: CA2682128414
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095705_27095706insATG , CM000669.2:g.27095705_27095706insATG GRCh38
NC_000007.13:g.27135324_27135325insATG , CM000669.1:g.27135324_27135325insATG GRCh37
NC_000007.12:g.27101849_27101850insATG NCBI36
NG_011813.1:g.5303_5304insTCA
NG_033087.1:g.4612_4613insATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.209_210insTCA MANE Select ENSP00000494260.2:p.His70_His71insHis
ENST00000343060.4:c.209_210insTCA ENSP00000343246.4:p.His70_His71insHis
ENST00000355633.5:c.209_210insTCA ENSP00000347851.5:p.His70_His71insHis
NM_005522.4:c.209_210insTCA NP_005513.1:p.His70_His71insHis
NM_153620.2:c.209_210insTCA NP_705873.2:p.His70_His71insHis
NM_005522.5:c.209_210insTCA MANE Select NP_005513.2:p.His70_His71insHis
NM_153620.3:c.209_210insTCA NP_705873.3:p.His70_His71insHis