Canonical Allele Identifier: CA2042242429

Gene: GNS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64728901A= , CM000674.2:g.64728901A=	GRCh38
NC_000012.11:g.65122681A= , CM000674.1:g.65122681A=	GRCh37
NC_000012.10:g.63408948A=	NCBI36
NG_008955.1:g.35546T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258145.8:c.1200+55T= MANE Select	ENSP00000258145.3:n.1200+55T=
ENST00000258145.7:c.1200+55T=	ENSP00000258145.3:n.1200+55T=
ENST00000418919.6:c.1032+55T=	ENSP00000413130.2:n.1032+55T=
ENST00000537823.1:n.199+55T=
ENST00000540196.5:c.557-5788T=
ENST00000540883.1:n.263+55T=
ENST00000541781.5:n.1255+55T=
ENST00000542058.5:c.1140+55T=	ENSP00000444819.1:n.1140+55T=
ENST00000543646.5:c.1296+55T=	ENSP00000438497.1:n.1296+55T=
NM_002076.3:c.1200+55T=	NP_002067.1:n.1200+55T=
NM_002076.4:c.1200+55T= MANE Select	NP_002067.1:n.1200+55T=