Canonical Allele Identifier: CA2338594612

Gene: SIX5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45767028G= , CM000681.2:g.45767028G=	GRCh38
NC_000019.9:g.46270286G= , CM000681.1:g.46270286G=	GRCh37
NC_000019.8:g.50962126G=	NCBI36
NG_012745.1:g.7212C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.931C= MANE Select	ENSP00000316842.4:p.Pro311=
ENST00000317578.6:c.931C=	ENSP00000316842.4:p.Pro311=
ENST00000560160.1:c.587-917C=
ENST00000560168.1:c.*119C=	ENSP00000453189.2:n.*119C=
ENST00000622857.1:c.16-1066C=	ENSP00000481365.1:n.16-1066C=
NM_175875.4:c.931C=	NP_787071.2:p.Pro311=
NM_175875.5:c.931C= MANE Select	NP_787071.3:p.Pro311=