Canonical Allele Identifier: CA1410031392

Gene: GYG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149009385C= , CM000665.2:g.149009385C=	GRCh38
NC_000003.11:g.148727172C= , CM000665.1:g.148727172C=	GRCh37
NC_000003.10:g.150209862C=	NCBI36
NG_027677.1:g.22978C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345003.9:c.591C= MANE Select	ENSP00000340736.4:p.Tyr197=
ENST00000296048.10:c.591C=	ENSP00000296048.6:p.Tyr197=
ENST00000345003.8:c.591C=	ENSP00000340736.4:p.Tyr197=
ENST00000461191.1:c.579C=	ENSP00000420247.1:p.Tyr193=
ENST00000469873.1:n.505C=
ENST00000479119.1:n.207C=
ENST00000483267.5:c.469+12493C=	ENSP00000419499.1:n.469+12493C=
ENST00000484197.5:c.591C=	ENSP00000420683.1:p.Tyr197=
ENST00000497528.5:n.230C=
ENST00000627418.2:c.469+12493C=	ENSP00000486061.1:n.469+12493C=
NM_001184720.1:c.591C=	NP_001171649.1:p.Tyr197=
NM_001184721.1:c.591C=	NP_001171650.1:p.Tyr197=
NM_004130.3:c.591C=	NP_004121.2:p.Tyr197=
XM_017006275.1:c.414C=	XP_016861764.1:p.Tyr138=
XM_017006276.1:c.129C=	XP_016861765.1:p.Tyr43=
NM_004130.4:c.591C= MANE Select	NP_004121.2:p.Tyr197=
NM_001184720.2:c.591C=	NP_001171649.1:p.Tyr197=
NM_001184721.2:c.591C=	NP_001171650.1:p.Tyr197=