Canonical Allele Identifier: CA1696186874
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1783795140

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095420del , CM000669.2:g.27095420del GRCh38
NC_000007.13:g.27135039del , CM000669.1:g.27135039del GRCh37
NC_000007.12:g.27101564del NCBI36
NG_011813.1:g.5588del
NG_033087.1:g.4327del

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.494del MANE Select ENSP00000494260.2:p.Gly165AspfsTer?
ENST00000343060.4:c.494del ENSP00000343246.4:p.Gly165AspfsTer?
ENST00000355633.5:c.355-64del ENSP00000347851.5:n.355-64del
NM_005522.4:c.494del NP_005513.1:p.Gly165AspfsTer?
NM_153620.2:c.355-64del NP_705873.2:n.355-64del
NM_005522.5:c.494del MANE Select NP_005513.2:p.Gly165AspfsTer?
NM_153620.3:c.355-64del NP_705873.3:n.355-64del