Canonical Allele Identifier: CA917969047
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1554333646

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095723dup , CM000669.2:g.27095723dup GRCh38
NC_000007.13:g.27135342dup , CM000669.1:g.27135342dup GRCh37
NC_000007.12:g.27101867dup NCBI36
NG_011813.1:g.5287dup
NG_033087.1:g.4630dup

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.193dup MANE Select ENSP00000494260.2:p.His65ProfsTer?
ENST00000343060.4:c.193dup ENSP00000343246.4:p.His65ProfsTer?
ENST00000355633.5:c.193dup ENSP00000347851.5:p.His65ProfsTer?
NM_005522.4:c.193dup NP_005513.1:p.His65ProfsTer?
NM_153620.2:c.193dup NP_705873.2:p.His65ProfsTer?
NM_005522.5:c.193dup MANE Select NP_005513.2:p.His65ProfsTer?
NM_153620.3:c.193dup NP_705873.3:p.His65ProfsTer?