Canonical Allele Identifier: CA573758420
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1184593662

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095694del , CM000669.2:g.27095694del GRCh38
NC_000007.13:g.27135313del , CM000669.1:g.27135313del GRCh37
NC_000007.12:g.27101838del NCBI36
NG_011813.1:g.5314del
NG_033087.1:g.4601del

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.220del MANE Select ENSP00000494260.2:p.His74ThrfsTer?
ENST00000343060.4:c.220del ENSP00000343246.4:p.His74ThrfsTer?
ENST00000355633.5:c.220del ENSP00000347851.5:p.His74ThrfsTer?
NM_005522.4:c.220del NP_005513.1:p.His74ThrfsTer?
NM_153620.2:c.220del NP_705873.2:p.His74ThrfsTer?
NM_005522.5:c.220del MANE Select NP_005513.2:p.His74ThrfsTer?
NM_153620.3:c.220del NP_705873.3:p.His74ThrfsTer?