Canonical Allele Identifier: CA367068804
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095582A>G , CM000669.2:g.27095582A>G GRCh38
NC_000007.13:g.27135201A>G , CM000669.1:g.27135201A>G GRCh37
NC_000007.12:g.27101726A>G NCBI36
NG_011813.1:g.5425T>C
NG_033087.1:g.4489A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.331T>C MANE Select ENSP00000494260.2:p.Tyr111His
ENST00000343060.4:c.331T>C ENSP00000343246.4:p.Tyr111His
ENST00000355633.5:c.331T>C ENSP00000347851.5:p.Tyr111His
NM_005522.4:c.331T>C NP_005513.1:p.Tyr111His
NM_153620.2:c.331T>C NP_705873.2:p.Tyr111His
NM_005522.5:c.331T>C MANE Select NP_005513.2:p.Tyr111His
NM_153620.3:c.331T>C NP_705873.3:p.Tyr111His