Canonical Allele Identifier: CA2042242573

Gene: GNS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64729008C= , CM000674.2:g.64729008C=	GRCh38
NC_000012.11:g.65122788C= , CM000674.1:g.65122788C=	GRCh37
NC_000012.10:g.63409055C=	NCBI36
NG_008955.1:g.35439G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258145.8:c.1148G= MANE Select	ENSP00000258145.3:p.Gly383=
ENST00000258145.7:c.1148G=	ENSP00000258145.3:p.Gly383=
ENST00000418919.6:c.980G=	ENSP00000413130.2:p.Gly327=
ENST00000537823.1:n.147G=
ENST00000540196.5:c.557-5895G=
ENST00000540883.1:n.211G=
ENST00000541781.5:n.1203G=
ENST00000542058.5:c.1088G=	ENSP00000444819.1:p.Gly363=
ENST00000543646.5:c.1244G=	ENSP00000438497.1:p.Gly415=
NM_002076.3:c.1148G=	NP_002067.1:p.Gly383=
NM_002076.4:c.1148G= MANE Select	NP_002067.1:p.Gly383=