Canonical Allele Identifier: CA2338594279

Gene: SIX5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45766484C= , CM000681.2:g.45766484C=	GRCh38
NC_000019.9:g.46269742C= , CM000681.1:g.46269742C=	GRCh37
NC_000019.8:g.50961582C=	NCBI36
NG_012745.1:g.7756G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.1475G= MANE Select	ENSP00000316842.4:p.Gly492=
ENST00000317578.6:c.1475G=	ENSP00000316842.4:p.Gly492=
ENST00000560160.1:c.587-373G=
ENST00000560168.1:c.*663G=	ENSP00000453189.2:n.*663G=
ENST00000622857.1:c.16-522G=	ENSP00000481365.1:n.16-522G=
NM_175875.4:c.1475G=	NP_787071.2:p.Gly492=
NM_175875.5:c.1475G= MANE Select	NP_787071.3:p.Gly492=