Canonical Allele Identifier: CA2668126431
Gene: GYG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149009158_149009159insG , CM000665.2:g.149009158_149009159insG GRCh38
NC_000003.11:g.148726945_148726946insG , CM000665.1:g.148726945_148726946insG GRCh37
NC_000003.10:g.150209635_150209636insG NCBI36
NG_027677.1:g.22751_22752insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000345003.9:c.482-118_482-117insG MANE Select ENSP00000340736.4:n.482-118_482-117insG
ENST00000296048.10:c.482-118_482-117insG ENSP00000296048.6:n.482-118_482-117insG
ENST00000345003.8:c.482-118_482-117insG ENSP00000340736.4:n.482-118_482-117insG
ENST00000461191.1:c.470-118_470-117insG ENSP00000420247.1:n.470-118_470-117insG
ENST00000469873.1:n.278_279insG
ENST00000479119.1:n.98-118_98-117insG
ENST00000483267.5:c.469+12266_469+12267insG ENSP00000419499.1:n.469+12266_469+12267insG
ENST00000484197.5:c.482-118_482-117insG ENSP00000420683.1:n.482-118_482-117insG
ENST00000497528.5:n.121-118_121-117insG
ENST00000627418.2:c.469+12266_469+12267insG ENSP00000486061.1:n.469+12266_469+12267insG
NM_001184720.1:c.482-118_482-117insG NP_001171649.1:n.482-118_482-117insG
NM_001184721.1:c.482-118_482-117insG NP_001171650.1:n.482-118_482-117insG
NM_004130.3:c.482-118_482-117insG NP_004121.2:n.482-118_482-117insG
XM_017006275.1:c.305-118_305-117insG XP_016861764.1:n.305-118_305-117insG
XM_017006276.1:c.20-118_20-117insG XP_016861765.1:n.20-118_20-117insG
NM_004130.4:c.482-118_482-117insG MANE Select NP_004121.2:n.482-118_482-117insG
NM_001184720.2:c.482-118_482-117insG NP_001171649.1:n.482-118_482-117insG
NM_001184721.2:c.482-118_482-117insG NP_001171650.1:n.482-118_482-117insG