Canonical Allele Identifier: CA1410022672

Gene: GYG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148994163C= , CM000665.2:g.148994163C=	GRCh38
NC_000003.11:g.148711950C= , CM000665.1:g.148711950C=	GRCh37
NC_000003.10:g.150194640C=	NCBI36
NG_027677.1:g.7756C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345003.9:c.29C= MANE Select	ENSP00000340736.4:p.Thr10=
ENST00000296048.10:c.29C=	ENSP00000296048.6:p.Thr10=
ENST00000345003.8:c.29C=	ENSP00000340736.4:p.Thr10=
ENST00000461191.1:c.29C=	ENSP00000420247.1:p.Thr10=
ENST00000473005.1:c.-110C=	ENSP00000417671.1:n.-110C=
ENST00000478067.1:n.130C=
ENST00000483267.5:c.29C=	ENSP00000419499.1:p.Thr10=
ENST00000484197.5:c.29C=	ENSP00000420683.1:p.Thr10=
ENST00000492285.6:c.-110C=	ENSP00000418297.2:n.-110C=
ENST00000627418.2:c.29C=	ENSP00000486061.1:p.Thr10=
NM_001184720.1:c.29C=	NP_001171649.1:p.Thr10=
NM_001184721.1:c.29C=	NP_001171650.1:p.Thr10=
NM_004130.3:c.29C=	NP_004121.2:p.Thr10=
XM_017006275.1:c.-34-2139C=	XP_016861764.1:n.-34-2139C=
NM_004130.4:c.29C= MANE Select	NP_004121.2:p.Thr10=
NM_001184720.2:c.29C=	NP_001171649.1:p.Thr10=
NM_001184721.2:c.29C=	NP_001171650.1:p.Thr10=