Canonical Allele Identifier: CA2841343593

Gene: GNS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64728900dup , CM000674.2:g.64728900dup	GRCh38
NC_000012.11:g.65122680dup , CM000674.1:g.65122680dup	GRCh37
NC_000012.10:g.63408947dup	NCBI36
NG_008955.1:g.35547dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258145.8:c.1200+56dup MANE Select	ENSP00000258145.3:n.1200+56dup
ENST00000258145.7:c.1200+56dup	ENSP00000258145.3:n.1200+56dup
ENST00000418919.6:c.1032+56dup	ENSP00000413130.2:n.1032+56dup
ENST00000537823.1:n.199+56dup
ENST00000540196.5:c.557-5787dup
ENST00000540883.1:n.263+56dup
ENST00000541781.5:n.1255+56dup
ENST00000542058.5:c.1140+56dup	ENSP00000444819.1:n.1140+56dup
ENST00000543646.5:c.1296+56dup	ENSP00000438497.1:n.1296+56dup
NM_002076.3:c.1200+56dup	NP_002067.1:n.1200+56dup
NM_002076.4:c.1200+56dup MANE Select	NP_002067.1:n.1200+56dup