Canonical Allele Identifier: CA2668126513
Gene: GYG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149009248A>T , CM000665.2:g.149009248A>T GRCh38
NC_000003.11:g.148727035A>T , CM000665.1:g.148727035A>T GRCh37
NC_000003.10:g.150209725A>T NCBI36
NG_027677.1:g.22841A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000345003.9:c.482-28A>T MANE Select ENSP00000340736.4:n.482-28A>T
ENST00000296048.10:c.482-28A>T ENSP00000296048.6:n.482-28A>T
ENST00000345003.8:c.482-28A>T ENSP00000340736.4:n.482-28A>T
ENST00000461191.1:c.470-28A>T ENSP00000420247.1:n.470-28A>T
ENST00000469873.1:n.368A>T
ENST00000479119.1:n.98-28A>T
ENST00000483267.5:c.469+12356A>T ENSP00000419499.1:n.469+12356A>T
ENST00000484197.5:c.482-28A>T ENSP00000420683.1:n.482-28A>T
ENST00000497528.5:n.121-28A>T
ENST00000627418.2:c.469+12356A>T ENSP00000486061.1:n.469+12356A>T
NM_001184720.1:c.482-28A>T NP_001171649.1:n.482-28A>T
NM_001184721.1:c.482-28A>T NP_001171650.1:n.482-28A>T
NM_004130.3:c.482-28A>T NP_004121.2:n.482-28A>T
XM_017006275.1:c.305-28A>T XP_016861764.1:n.305-28A>T
XM_017006276.1:c.20-28A>T XP_016861765.1:n.20-28A>T
NM_004130.4:c.482-28A>T MANE Select NP_004121.2:n.482-28A>T
NM_001184720.2:c.482-28A>T NP_001171649.1:n.482-28A>T
NM_001184721.2:c.482-28A>T NP_001171650.1:n.482-28A>T