Canonical Allele Identifier: CA354910344

Gene: GYG1

Linked Data

• MyVariant Identifiers: chr3:g.148712049T>G (hg19) ; chr3:g.148994262T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148994262T>G , CM000665.2:g.148994262T>G	GRCh38
NC_000003.11:g.148712049T>G , CM000665.1:g.148712049T>G	GRCh37
NC_000003.10:g.150194739T>G	NCBI36
NG_027677.1:g.7855T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000345003.9:c.128T>G MANE Select	ENSP00000340736.4:p.Val43Gly
ENST00000296048.10:c.128T>G	ENSP00000296048.6:p.Val43Gly
ENST00000345003.8:c.128T>G	ENSP00000340736.4:p.Val43Gly
ENST00000461191.1:c.128T>G	ENSP00000420247.1:p.Val43Gly
ENST00000465547.1:n.49+2T>G
ENST00000473005.1:c.-11T>G	ENSP00000417671.1:n.-11T>G
ENST00000478067.1:n.229T>G
ENST00000483267.5:c.128T>G	ENSP00000419499.1:p.Val43Gly
ENST00000484197.5:c.128T>G	ENSP00000420683.1:p.Val43Gly
ENST00000492285.6:c.-11T>G	ENSP00000418297.2:n.-11T>G
ENST00000627418.2:c.128T>G	ENSP00000486061.1:p.Val43Gly
NM_001184720.1:c.128T>G	NP_001171649.1:p.Val43Gly
NM_001184721.1:c.128T>G	NP_001171650.1:p.Val43Gly
NM_004130.3:c.128T>G	NP_004121.2:p.Val43Gly
XM_017006275.1:c.-34-2040T>G	XP_016861764.1:n.-34-2040T>G
NM_004130.4:c.128T>G MANE Select	NP_004121.2:p.Val43Gly
NM_001184720.2:c.128T>G	NP_001171649.1:p.Val43Gly
NM_001184721.2:c.128T>G	NP_001171650.1:p.Val43Gly