Canonical Allele Identifier: CA2578852732
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095462dup , CM000669.2:g.27095462dup GRCh38
NC_000007.13:g.27135081dup , CM000669.1:g.27135081dup GRCh37
NC_000007.12:g.27101606dup NCBI36
NG_011813.1:g.5549dup
NG_033087.1:g.4369dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.455dup MANE Select ENSP00000494260.2:p.Ala153ArgfsTer25
ENST00000343060.4:c.455dup ENSP00000343246.4:p.Ala153ArgfsTer25
ENST00000355633.5:c.354+101dup ENSP00000347851.5:n.354+101dup
NM_005522.4:c.455dup NP_005513.1:p.Ala153ArgfsTer25
NM_153620.2:c.354+101dup NP_705873.2:n.354+101dup
NM_005522.5:c.455dup MANE Select NP_005513.2:p.Ala153ArgfsTer25
NM_153620.3:c.354+101dup NP_705873.3:n.354+101dup