Canonical Allele Identifier: CA367068402
Gene: HOXA1 HGNC NCBI

Linked Data

COSMIC: COSM746326

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095399C>A , CM000669.2:g.27095399C>A GRCh38
NC_000007.13:g.27135018C>A , CM000669.1:g.27135018C>A GRCh37
NC_000007.12:g.27101543C>A NCBI36
NG_011813.1:g.5608G>T
NG_033087.1:g.4306C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.514G>T MANE Select ENSP00000494260.2:p.Ala172Ser
ENST00000343060.4:c.514G>T ENSP00000343246.4:p.Ala172Ser
ENST00000355633.5:c.355-44G>T ENSP00000347851.5:n.355-44G>T
NM_005522.4:c.514G>T NP_005513.1:p.Ala172Ser
NM_153620.2:c.355-44G>T NP_705873.2:n.355-44G>T
NM_005522.5:c.514G>T MANE Select NP_005513.2:p.Ala172Ser
NM_153620.3:c.355-44G>T NP_705873.3:n.355-44G>T