Canonical Allele Identifier: CA573758421
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1369656027

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095694_27095696del , CM000669.2:g.27095694_27095696del GRCh38
NC_000007.13:g.27135313_27135315del , CM000669.1:g.27135313_27135315del GRCh37
NC_000007.12:g.27101838_27101840del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.218_220del MANE Select ENSP00000494260.2:p.Arg73del
ENST00000343060.4:c.218_220del ENSP00000343246.4:p.Arg73del
ENST00000355633.5:c.218_220del ENSP00000347851.5:p.Arg73del
NM_005522.5:c.218_220del MANE Select NP_005513.2:p.Arg73del
NM_153620.3:c.218_220del NP_705873.3:p.Arg73del