Canonical Allele Identifier: CA2338594565
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766948G= , CM000681.2:g.45766948G= GRCh38
NC_000019.9:g.46270206G= , CM000681.1:g.46270206G= GRCh37
NC_000019.8:g.50962046G= NCBI36
NG_012745.1:g.7292C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1011C= MANE Select ENSP00000316842.4:p.Leu337=
ENST00000317578.6:c.1011C= ENSP00000316842.4:p.Leu337=
ENST00000560160.1:c.587-837C=
ENST00000560168.1:c.*199C= ENSP00000453189.2:n.*199C=
ENST00000622857.1:c.16-986C= ENSP00000481365.1:n.16-986C=
NM_175875.4:c.1011C= NP_787071.2:p.Leu337=
NM_175875.5:c.1011C= MANE Select NP_787071.3:p.Leu337=