Canonical Allele Identifier: CA367068667
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095520G>C , CM000669.2:g.27095520G>C GRCh38
NC_000007.13:g.27135139G>C , CM000669.1:g.27135139G>C GRCh37
NC_000007.12:g.27101664G>C NCBI36
NG_011813.1:g.5487C>G
NG_033087.1:g.4427G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.393C>G MANE Select ENSP00000494260.2:p.Tyr131Ter
ENST00000343060.4:c.393C>G ENSP00000343246.4:p.Tyr131Ter
ENST00000355633.5:c.354+39C>G ENSP00000347851.5:n.354+39C>G
NM_005522.4:c.393C>G NP_005513.1:p.Tyr131Ter
NM_153620.2:c.354+39C>G NP_705873.2:n.354+39C>G
NM_005522.5:c.393C>G MANE Select NP_005513.2:p.Tyr131Ter
NM_153620.3:c.354+39C>G NP_705873.3:n.354+39C>G