Canonical Allele Identifier: CA2042242654

Gene: GNS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64729045T= , CM000674.2:g.64729045T=	GRCh38
NC_000012.11:g.65122825T= , CM000674.1:g.65122825T=	GRCh37
NC_000012.10:g.63409092T=	NCBI36
NG_008955.1:g.35402A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258145.8:c.1111A= MANE Select	ENSP00000258145.3:p.Asn371=
ENST00000258145.7:c.1111A=	ENSP00000258145.3:p.Asn371=
ENST00000418919.6:c.943A=	ENSP00000413130.2:p.Asn315=
ENST00000537823.1:n.110A=
ENST00000540196.5:c.557-5932A=
ENST00000540883.1:n.174A=
ENST00000541781.5:n.1166A=
ENST00000542058.5:c.1051A=	ENSP00000444819.1:p.Asn351=
ENST00000543646.5:c.1207A=	ENSP00000438497.1:p.Asn403=
NM_002076.3:c.1111A=	NP_002067.1:p.Asn371=
NM_002076.4:c.1111A= MANE Select	NP_002067.1:p.Asn371=