Canonical Allele Identifier: CA6669742

Gene: GNS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64729009C>T , CM000674.2:g.64729009C>T	GRCh38
NC_000012.11:g.65122789C>T , CM000674.1:g.65122789C>T	GRCh37
NC_000012.10:g.63409056C>T	NCBI36
NG_008955.1:g.35438G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002076.4:c.1147G>A MANE Select	NP_002067.1:p.Gly383Ser
ENST00000258145.8:c.1147G>A MANE Select	ENSP00000258145.3:p.Gly383Ser
NM_002076.3:c.1147G>A	NP_002067.1:p.Gly383Ser
ENST00000258145.7:c.1147G>A	ENSP00000258145.3:p.Gly383Ser
ENST00000418919.6:c.979G>A	ENSP00000413130.2:p.Gly327Ser
ENST00000537823.1:n.146G>A
ENST00000540196.5:c.557-5896G>A
ENST00000540883.1:n.210G>A
ENST00000541781.5:n.1202G>A
ENST00000542058.5:c.1087G>A	ENSP00000444819.1:p.Gly363Ser
ENST00000543646.5:c.1243G>A	ENSP00000438497.1:p.Gly415Ser