Canonical Allele Identifier: CA2578852733
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095467dup , CM000669.2:g.27095467dup GRCh38
NC_000007.13:g.27135086dup , CM000669.1:g.27135086dup GRCh37
NC_000007.12:g.27101611dup NCBI36
NG_011813.1:g.5540dup
NG_033087.1:g.4374dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.446dup MANE Select ENSP00000494260.2:p.Tyr149Ter
ENST00000343060.4:c.446dup ENSP00000343246.4:p.Tyr149Ter
ENST00000355633.5:c.354+92dup ENSP00000347851.5:n.354+92dup
NM_005522.4:c.446dup NP_005513.1:p.Tyr149Ter
NM_153620.2:c.354+92dup NP_705873.2:n.354+92dup
NM_005522.5:c.446dup MANE Select NP_005513.2:p.Tyr149Ter
NM_153620.3:c.354+92dup NP_705873.3:n.354+92dup