Canonical Allele Identifier: CA1410031337

Gene: GYG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149009271T= , CM000665.2:g.149009271T=	GRCh38
NC_000003.11:g.148727058T= , CM000665.1:g.148727058T=	GRCh37
NC_000003.10:g.150209748T=	NCBI36
NG_027677.1:g.22864T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000345003.9:c.482-5T= MANE Select	ENSP00000340736.4:n.482-5T=
ENST00000296048.10:c.482-5T=	ENSP00000296048.6:n.482-5T=
ENST00000345003.8:c.482-5T=	ENSP00000340736.4:n.482-5T=
ENST00000461191.1:c.470-5T=	ENSP00000420247.1:n.470-5T=
ENST00000469873.1:n.391T=
ENST00000479119.1:n.98-5T=
ENST00000483267.5:c.469+12379T=	ENSP00000419499.1:n.469+12379T=
ENST00000484197.5:c.482-5T=	ENSP00000420683.1:n.482-5T=
ENST00000497528.5:n.121-5T=
ENST00000627418.2:c.469+12379T=	ENSP00000486061.1:n.469+12379T=
NM_001184720.1:c.482-5T=	NP_001171649.1:n.482-5T=
NM_001184721.1:c.482-5T=	NP_001171650.1:n.482-5T=
NM_004130.3:c.482-5T=	NP_004121.2:n.482-5T=
XM_017006275.1:c.305-5T=	XP_016861764.1:n.305-5T=
XM_017006276.1:c.20-5T=	XP_016861765.1:n.20-5T=
NM_004130.4:c.482-5T= MANE Select	NP_004121.2:n.482-5T=
NM_001184720.2:c.482-5T=	NP_001171649.1:n.482-5T=
NM_001184721.2:c.482-5T=	NP_001171650.1:n.482-5T=