Canonical Allele Identifier: CA2338594442

Gene: SIX5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45766749C= , CM000681.2:g.45766749C=	GRCh38
NC_000019.9:g.46270007C= , CM000681.1:g.46270007C=	GRCh37
NC_000019.8:g.50961847C=	NCBI36
NG_012745.1:g.7491G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.1210G= MANE Select	ENSP00000316842.4:p.Glu404=
ENST00000317578.6:c.1210G=	ENSP00000316842.4:p.Glu404=
ENST00000560160.1:c.587-638G=
ENST00000560168.1:c.*398G=	ENSP00000453189.2:n.*398G=
ENST00000622857.1:c.16-787G=	ENSP00000481365.1:n.16-787G=
NM_175875.4:c.1210G=	NP_787071.2:p.Glu404=
NM_175875.5:c.1210G= MANE Select	NP_787071.3:p.Glu404=