Canonical Allele Identifier: CA1696186872
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095418_27095419delinsTC , CM000669.2:g.27095418_27095419delinsTC GRCh38
NC_000007.13:g.27135037_27135038delinsTC , CM000669.1:g.27135037_27135038delinsTC GRCh37
NC_000007.12:g.27101562_27101563delinsTC NCBI36
NG_011813.1:g.5588_5589delinsGA
NG_033087.1:g.4325_4326delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.494_495delinsGA MANE Select ENSP00000494260.2:p.Gly165=
ENST00000343060.4:c.494_495delinsGA ENSP00000343246.4:p.Gly165=
ENST00000355633.5:c.355-64_355-63delinsGA ENSP00000347851.5:n.355-64_355-63delinsGA
NM_005522.4:c.494_495delinsGA NP_005513.1:p.Gly165=
NM_153620.2:c.355-64_355-63delinsGA NP_705873.2:n.355-64_355-63delinsGA
NM_005522.5:c.494_495delinsGA MANE Select NP_005513.2:p.Gly165=
NM_153620.3:c.355-64_355-63delinsGA NP_705873.3:n.355-64_355-63delinsGA