Canonical Allele Identifier: CA1410022669

Gene: GYG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148994155G= , CM000665.2:g.148994155G=	GRCh38
NC_000003.11:g.148711942G= , CM000665.1:g.148711942G=	GRCh37
NC_000003.10:g.150194632G=	NCBI36
NG_027677.1:g.7748G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000345003.9:c.21G= MANE Select	ENSP00000340736.4:p.Val7=
ENST00000296048.10:c.21G=	ENSP00000296048.6:p.Val7=
ENST00000345003.8:c.21G=	ENSP00000340736.4:p.Val7=
ENST00000461191.1:c.21G=	ENSP00000420247.1:p.Val7=
ENST00000473005.1:c.-118G=	ENSP00000417671.1:n.-118G=
ENST00000478067.1:n.122G=
ENST00000483267.5:c.21G=	ENSP00000419499.1:p.Val7=
ENST00000484197.5:c.21G=	ENSP00000420683.1:p.Val7=
ENST00000492285.6:c.-118G=	ENSP00000418297.2:n.-118G=
ENST00000627418.2:c.21G=	ENSP00000486061.1:p.Val7=
NM_001184720.1:c.21G=	NP_001171649.1:p.Val7=
NM_001184721.1:c.21G=	NP_001171650.1:p.Val7=
NM_004130.3:c.21G=	NP_004121.2:p.Val7=
XM_017006275.1:c.-34-2147G=	XP_016861764.1:n.-34-2147G=
NM_004130.4:c.21G= MANE Select	NP_004121.2:p.Val7=
NM_001184720.2:c.21G=	NP_001171649.1:p.Val7=
NM_001184721.2:c.21G=	NP_001171650.1:p.Val7=