Canonical Allele Identifier: CA436197249

Gene: GYG1

Linked Data

• MyVariant Identifiers: chr3:g.148727115T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149009328T>C , CM000665.2:g.149009328T>C	GRCh38
NC_000003.11:g.148727115T>C , CM000665.1:g.148727115T>C	GRCh37
NC_000003.10:g.150209805T>C	NCBI36
NG_027677.1:g.22921T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345003.9:c.534T>C MANE Select	ENSP00000340736.4:p.Asp178=
ENST00000296048.10:c.534T>C	ENSP00000296048.6:p.Asp178=
ENST00000345003.8:c.534T>C	ENSP00000340736.4:p.Asp178=
ENST00000461191.1:c.522T>C	ENSP00000420247.1:p.Asp174=
ENST00000469873.1:n.448T>C
ENST00000479119.1:n.150T>C
ENST00000483267.5:c.469+12436T>C	ENSP00000419499.1:n.469+12436T>C
ENST00000484197.5:c.534T>C	ENSP00000420683.1:p.Asp178=
ENST00000497528.5:n.173T>C
ENST00000627418.2:c.469+12436T>C	ENSP00000486061.1:n.469+12436T>C
NM_001184720.1:c.534T>C	NP_001171649.1:p.Asp178=
NM_001184721.1:c.534T>C	NP_001171650.1:p.Asp178=
NM_004130.3:c.534T>C	NP_004121.2:p.Asp178=
XM_017006275.1:c.357T>C	XP_016861764.1:p.Asp119=
XM_017006276.1:c.72T>C	XP_016861765.1:p.Asp24=
NM_004130.4:c.534T>C MANE Select	NP_004121.2:p.Asp178=
NM_001184720.2:c.534T>C	NP_001171649.1:p.Asp178=
NM_001184721.2:c.534T>C	NP_001171650.1:p.Asp178=