Canonical Allele Identifier: CA1410022674

Gene: GYG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148994166_148994167delinsCA , CM000665.2:g.148994166_148994167delinsCA	GRCh38
NC_000003.11:g.148711953_148711954delinsCA , CM000665.1:g.148711953_148711954delinsCA	GRCh37
NC_000003.10:g.150194643_150194644delinsCA	NCBI36
NG_027677.1:g.7759_7760delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345003.9:c.32_33delinsCA MANE Select	ENSP00000340736.4:p.Thr11=
ENST00000296048.10:c.32_33delinsCA	ENSP00000296048.6:p.Thr11=
ENST00000345003.8:c.32_33delinsCA	ENSP00000340736.4:p.Thr11=
ENST00000461191.1:c.32_33delinsCA	ENSP00000420247.1:p.Thr11=
ENST00000473005.1:c.-107_-106delinsCA	ENSP00000417671.1:n.-107_-106delinsCA
ENST00000478067.1:n.133_134delinsCA
ENST00000483267.5:c.32_33delinsCA	ENSP00000419499.1:p.Thr11=
ENST00000484197.5:c.32_33delinsCA	ENSP00000420683.1:p.Thr11=
ENST00000492285.6:c.-107_-106delinsCA	ENSP00000418297.2:n.-107_-106delinsCA
ENST00000627418.2:c.32_33delinsCA	ENSP00000486061.1:p.Thr11=
NM_001184720.1:c.32_33delinsCA	NP_001171649.1:p.Thr11=
NM_001184721.1:c.32_33delinsCA	NP_001171650.1:p.Thr11=
NM_004130.3:c.32_33delinsCA	NP_004121.2:p.Thr11=
XM_017006275.1:c.-34-2136_-34-2135delinsCA	XP_016861764.1:n.-34-2136_-34-2135delinsCA
NM_004130.4:c.32_33delinsCA MANE Select	NP_004121.2:p.Thr11=
NM_001184720.2:c.32_33delinsCA	NP_001171649.1:p.Thr11=
NM_001184721.2:c.32_33delinsCA	NP_001171650.1:p.Thr11=