Canonical Allele Identifier: CA436196948

Gene: GYG1

Linked Data

• gnomAD v4: 3-149009298-C-T
• MyVariant Identifiers: chr3:g.148727085C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149009298C>T , CM000665.2:g.149009298C>T	GRCh38
NC_000003.11:g.148727085C>T , CM000665.1:g.148727085C>T	GRCh37
NC_000003.10:g.150209775C>T	NCBI36
NG_027677.1:g.22891C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345003.9:c.504C>T MANE Select	ENSP00000340736.4:p.Asn168=
ENST00000296048.10:c.504C>T	ENSP00000296048.6:p.Asn168=
ENST00000345003.8:c.504C>T	ENSP00000340736.4:p.Asn168=
ENST00000461191.1:c.492C>T	ENSP00000420247.1:p.Asn164=
ENST00000469873.1:n.418C>T
ENST00000479119.1:n.120C>T
ENST00000483267.5:c.469+12406C>T	ENSP00000419499.1:n.469+12406C>T
ENST00000484197.5:c.504C>T	ENSP00000420683.1:p.Asn168=
ENST00000497528.5:n.143C>T
ENST00000627418.2:c.469+12406C>T	ENSP00000486061.1:n.469+12406C>T
NM_001184720.1:c.504C>T	NP_001171649.1:p.Asn168=
NM_001184721.1:c.504C>T	NP_001171650.1:p.Asn168=
NM_004130.3:c.504C>T	NP_004121.2:p.Asn168=
XM_017006275.1:c.327C>T	XP_016861764.1:p.Asn109=
XM_017006276.1:c.42C>T	XP_016861765.1:p.Asn14=
NM_004130.4:c.504C>T MANE Select	NP_004121.2:p.Asn168=
NM_001184720.2:c.504C>T	NP_001171649.1:p.Asn168=
NM_001184721.2:c.504C>T	NP_001171650.1:p.Asn168=