Canonical Allele Identifier: CA1696187399
Gene: HOXA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095727_27095728delinsAC , CM000669.2:g.27095727_27095728delinsAC GRCh38
NC_000007.13:g.27135346_27135347delinsAC , CM000669.1:g.27135346_27135347delinsAC GRCh37
NC_000007.12:g.27101871_27101872delinsAC NCBI36
NG_011813.1:g.5279_5280delinsGT
NG_033087.1:g.4634_4635delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.185_186delinsGT MANE Select ENSP00000494260.2:p.Gly62=
ENST00000343060.4:c.185_186delinsGT ENSP00000343246.4:p.Gly62=
ENST00000355633.5:c.185_186delinsGT ENSP00000347851.5:p.Gly62=
NM_005522.4:c.185_186delinsGT NP_005513.1:p.Gly62=
NM_153620.2:c.185_186delinsGT NP_705873.2:p.Gly62=
NM_005522.5:c.185_186delinsGT MANE Select NP_005513.2:p.Gly62=
NM_153620.3:c.185_186delinsGT NP_705873.3:p.Gly62=
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