Canonical Allele Identifier: CA2338594318
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766552G= , CM000681.2:g.45766552G= GRCh38
NC_000019.9:g.46269810G= , CM000681.1:g.46269810G= GRCh37
NC_000019.8:g.50961650G= NCBI36
NG_012745.1:g.7688C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1407C= MANE Select ENSP00000316842.4:p.Thr469=
ENST00000317578.6:c.1407C= ENSP00000316842.4:p.Thr469=
ENST00000560160.1:c.587-441C=
ENST00000560168.1:c.*595C= ENSP00000453189.2:n.*595C=
ENST00000622857.1:c.16-590C= ENSP00000481365.1:n.16-590C=
NM_175875.4:c.1407C= NP_787071.2:p.Thr469=
NM_175875.5:c.1407C= MANE Select NP_787071.3:p.Thr469=