Canonical Allele Identifier: CA2042242711

Gene: GNS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64729109T= , CM000674.2:g.64729109T=	GRCh38
NC_000012.11:g.65122889T= , CM000674.1:g.65122889T=	GRCh37
NC_000012.10:g.63409156T=	NCBI36
NG_008955.1:g.35338A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258145.8:c.1099-52A= MANE Select	ENSP00000258145.3:n.1099-52A=
ENST00000258145.7:c.1099-52A=	ENSP00000258145.3:n.1099-52A=
ENST00000418919.6:c.931-52A=	ENSP00000413130.2:n.931-52A=
ENST00000537823.1:n.46A=
ENST00000540196.5:c.557-5996A=
ENST00000540883.1:n.110A=
ENST00000541781.5:n.1154-52A=
ENST00000542058.5:c.1039-52A=	ENSP00000444819.1:n.1039-52A=
ENST00000543646.5:c.1195-52A=	ENSP00000438497.1:n.1195-52A=
NM_002076.3:c.1099-52A=	NP_002067.1:n.1099-52A=
NM_002076.4:c.1099-52A= MANE Select	NP_002067.1:n.1099-52A=