Canonical Allele Identifier: CA85504834

Gene: GYG1

Linked Data

• ClinVar Variation Id: 1206778
• ClinVar RCV Id: RCV001574537
• dbSNP Id: rs76917162
• gnomAD v2: 3-148727445-A-G
• gnomAD v3: 3-149009658-A-G
• gnomAD v4: 3-149009658-A-G
• MyVariant Identifiers: chr3:g.148727445A>G (hg19) ; chr3:g.149009658A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149009658A>G , CM000665.2:g.149009658A>G	GRCh38
NC_000003.11:g.148727445A>G , CM000665.1:g.148727445A>G	GRCh37
NC_000003.10:g.150210135A>G	NCBI36
NG_027677.1:g.23251A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345003.9:c.608+256A>G MANE Select	ENSP00000340736.4:n.608+256A>G
ENST00000296048.10:c.608+256A>G	ENSP00000296048.6:n.608+256A>G
ENST00000345003.8:c.608+256A>G	ENSP00000340736.4:n.608+256A>G
ENST00000461191.1:c.596+256A>G	ENSP00000420247.1:n.596+256A>G
ENST00000469873.1:n.522+256A>G
ENST00000479119.1:n.224+256A>G
ENST00000483267.5:c.469+12766A>G	ENSP00000419499.1:n.469+12766A>G
ENST00000484197.5:c.608+256A>G	ENSP00000420683.1:n.608+256A>G
ENST00000627418.2:c.469+12766A>G	ENSP00000486061.1:n.469+12766A>G
NM_001184720.1:c.608+256A>G	NP_001171649.1:n.608+256A>G
NM_001184721.1:c.608+256A>G	NP_001171650.1:n.608+256A>G
NM_004130.3:c.608+256A>G	NP_004121.2:n.608+256A>G
XM_017006275.1:c.431+256A>G	XP_016861764.1:n.431+256A>G
XM_017006276.1:c.146+256A>G	XP_016861765.1:n.146+256A>G
NM_004130.4:c.608+256A>G MANE Select	NP_004121.2:n.608+256A>G
NM_001184720.2:c.608+256A>G	NP_001171649.1:n.608+256A>G
NM_001184721.2:c.608+256A>G	NP_001171650.1:n.608+256A>G