Canonical Allele Identifier: CA1696187035
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095587C= , CM000669.2:g.27095587C= GRCh38
NC_000007.13:g.27135206C= , CM000669.1:g.27135206C= GRCh37
NC_000007.12:g.27101731C= NCBI36
NG_011813.1:g.5420G=
NG_033087.1:g.4494C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.326G= MANE Select ENSP00000494260.2:p.Ser109=
ENST00000343060.4:c.326G= ENSP00000343246.4:p.Ser109=
ENST00000355633.5:c.326G= ENSP00000347851.5:p.Ser109=
NM_005522.4:c.326G= NP_005513.1:p.Ser109=
NM_153620.2:c.326G= NP_705873.2:p.Ser109=
NM_005522.5:c.326G= MANE Select NP_005513.2:p.Ser109=
NM_153620.3:c.326G= NP_705873.3:p.Ser109=