Canonical Allele Identifier: CA2338594584
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766986C= , CM000681.2:g.45766986C= GRCh38
NC_000019.9:g.46270244C= , CM000681.1:g.46270244C= GRCh37
NC_000019.8:g.50962084C= NCBI36
NG_012745.1:g.7254G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.973G= MANE Select ENSP00000316842.4:p.Gly325=
ENST00000317578.6:c.973G= ENSP00000316842.4:p.Gly325=
ENST00000560160.1:c.587-875G=
ENST00000560168.1:c.*161G= ENSP00000453189.2:n.*161G=
ENST00000622857.1:c.16-1024G= ENSP00000481365.1:n.16-1024G=
NM_175875.4:c.973G= NP_787071.2:p.Gly325=
NM_175875.5:c.973G= MANE Select NP_787071.3:p.Gly325=