Canonical Allele Identifier: CA1696187267
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1783807444

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095697_27095705dup , CM000669.2:g.27095697_27095705dup GRCh38
NC_000007.13:g.27135316_27135324dup , CM000669.1:g.27135316_27135324dup GRCh37
NC_000007.12:g.27101841_27101849dup NCBI36
NG_011813.1:g.5303_5311dup
NG_033087.1:g.4604_4612dup

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.209_217dup MANE Select ENSP00000494260.2:p.His72_Arg73insHisHisH...
ENST00000343060.4:c.209_217dup ENSP00000343246.4:p.His72_Arg73insHisHisH...
ENST00000355633.5:c.209_217dup ENSP00000347851.5:p.His72_Arg73insHisHisH...
NM_005522.4:c.209_217dup NP_005513.1:p.His73_His74insHisHisHis
NM_153620.2:c.209_217dup NP_705873.2:p.His73_His74insHisHisHis
NM_005522.5:c.209_217dup MANE Select NP_005513.2:p.His72_Arg73insHisHisHis
NM_153620.3:c.209_217dup NP_705873.3:p.His72_Arg73insHisHisHis