Canonical Allele Identifier: CA1696187269
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095697_27095706delinsATGGTGGTGG , CM000669.2:g.27095697_27095706delinsATGGTGGTGG GRCh38
NC_000007.13:g.27135316_27135325delinsATGGTGGTGG , CM000669.1:g.27135316_27135325delinsATGGTGGTGG GRCh37
NC_000007.12:g.27101841_27101850delinsATGGTGGTGG NCBI36
NG_011813.1:g.5301_5310delinsCCACCACCAT
NG_033087.1:g.4604_4613delinsATGGTGGTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.207_216delinsCCACCACCAT MANE Select ENSP00000494260.2:p.His69=
ENST00000343060.4:c.207_216delinsCCACCACCAT ENSP00000343246.4:p.His69=
ENST00000355633.5:c.207_216delinsCCACCACCAT ENSP00000347851.5:p.His69=
NM_005522.4:c.207_216delinsCCACCACCAT NP_005513.1:p.His69=
NM_153620.2:c.207_216delinsCCACCACCAT NP_705873.2:p.His69=
NM_005522.5:c.207_216delinsCCACCACCAT MANE Select NP_005513.2:p.His69=
NM_153620.3:c.207_216delinsCCACCACCAT NP_705873.3:p.His69=