Canonical Allele Identifier: CA1410031331

Gene: GYG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149009260T= , CM000665.2:g.149009260T=	GRCh38
NC_000003.11:g.148727047T= , CM000665.1:g.148727047T=	GRCh37
NC_000003.10:g.150209737T=	NCBI36
NG_027677.1:g.22853T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000345003.9:c.482-16T= MANE Select	ENSP00000340736.4:n.482-16T=
ENST00000296048.10:c.482-16T=	ENSP00000296048.6:n.482-16T=
ENST00000345003.8:c.482-16T=	ENSP00000340736.4:n.482-16T=
ENST00000461191.1:c.470-16T=	ENSP00000420247.1:n.470-16T=
ENST00000469873.1:n.380T=
ENST00000479119.1:n.98-16T=
ENST00000483267.5:c.469+12368T=	ENSP00000419499.1:n.469+12368T=
ENST00000484197.5:c.482-16T=	ENSP00000420683.1:n.482-16T=
ENST00000497528.5:n.121-16T=
ENST00000627418.2:c.469+12368T=	ENSP00000486061.1:n.469+12368T=
NM_001184720.1:c.482-16T=	NP_001171649.1:n.482-16T=
NM_001184721.1:c.482-16T=	NP_001171650.1:n.482-16T=
NM_004130.3:c.482-16T=	NP_004121.2:n.482-16T=
XM_017006275.1:c.305-16T=	XP_016861764.1:n.305-16T=
XM_017006276.1:c.20-16T=	XP_016861765.1:n.20-16T=
NM_004130.4:c.482-16T= MANE Select	NP_004121.2:n.482-16T=
NM_001184720.2:c.482-16T=	NP_001171649.1:n.482-16T=
NM_001184721.2:c.482-16T=	NP_001171650.1:n.482-16T=