Canonical Allele Identifier: CA2338594592

Gene: SIX5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45767003G= , CM000681.2:g.45767003G=	GRCh38
NC_000019.9:g.46270261G= , CM000681.1:g.46270261G=	GRCh37
NC_000019.8:g.50962101G=	NCBI36
NG_012745.1:g.7237C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.956C= MANE Select	ENSP00000316842.4:p.Ser319=
ENST00000317578.6:c.956C=	ENSP00000316842.4:p.Ser319=
ENST00000560160.1:c.587-892C=
ENST00000560168.1:c.*144C=	ENSP00000453189.2:n.*144C=
ENST00000622857.1:c.16-1041C=	ENSP00000481365.1:n.16-1041C=
NM_175875.4:c.956C=	NP_787071.2:p.Ser319=
NM_175875.5:c.956C= MANE Select	NP_787071.3:p.Ser319=