Canonical Allele Identifier: CA2338594514
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766862C= , CM000681.2:g.45766862C= GRCh38
NC_000019.9:g.46270120C= , CM000681.1:g.46270120C= GRCh37
NC_000019.8:g.50961960C= NCBI36
NG_012745.1:g.7378G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1097G= MANE Select ENSP00000316842.4:p.Gly366=
ENST00000317578.6:c.1097G= ENSP00000316842.4:p.Gly366=
ENST00000560160.1:c.587-751G=
ENST00000560168.1:c.*285G= ENSP00000453189.2:n.*285G=
ENST00000622857.1:c.16-900G= ENSP00000481365.1:n.16-900G=
NM_175875.4:c.1097G= NP_787071.2:p.Gly366=
NM_175875.5:c.1097G= MANE Select NP_787071.3:p.Gly366=