Canonical Allele Identifier: CA1696187289
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs747464910

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095704_27095721dup , CM000669.2:g.27095704_27095721dup GRCh38
NC_000007.13:g.27135323_27135340dup , CM000669.1:g.27135323_27135340dup GRCh37
NC_000007.12:g.27101848_27101865dup NCBI36
NG_011813.1:g.5292_5309dup
NG_033087.1:g.4611_4628dup

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.198_215dup MANE Select ENSP00000494260.2:p.His72_Arg73insHisHisH...
ENST00000343060.4:c.198_215dup ENSP00000343246.4:p.His72_Arg73insHisHisH...
ENST00000355633.5:c.198_215dup ENSP00000347851.5:p.His72_Arg73insHisHisH...
NM_005522.4:c.198_215dup NP_005513.1:p.His72_His73insHisHisHisHisH...
NM_153620.2:c.198_215dup NP_705873.2:p.His72_His73insHisHisHisHisH...
NM_005522.5:c.198_215dup MANE Select NP_005513.2:p.His72_Arg73insHisHisHisHisH...
NM_153620.3:c.198_215dup NP_705873.3:p.His72_Arg73insHisHisHisHisH...