Canonical Allele Identifier: CA2605384413
Gene: GYG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149009148G>C , CM000665.2:g.149009148G>C GRCh38
NC_000003.11:g.148726935G>C , CM000665.1:g.148726935G>C GRCh37
NC_000003.10:g.150209625G>C NCBI36
NG_027677.1:g.22741G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000345003.9:c.482-128G>C MANE Select ENSP00000340736.4:n.482-128G>C
ENST00000296048.10:c.482-128G>C ENSP00000296048.6:n.482-128G>C
ENST00000345003.8:c.482-128G>C ENSP00000340736.4:n.482-128G>C
ENST00000461191.1:c.470-128G>C ENSP00000420247.1:n.470-128G>C
ENST00000469873.1:n.268G>C
ENST00000479119.1:n.98-128G>C
ENST00000483267.5:c.469+12256G>C ENSP00000419499.1:n.469+12256G>C
ENST00000484197.5:c.482-128G>C ENSP00000420683.1:n.482-128G>C
ENST00000497528.5:n.121-128G>C
ENST00000627418.2:c.469+12256G>C ENSP00000486061.1:n.469+12256G>C
NM_001184720.1:c.482-128G>C NP_001171649.1:n.482-128G>C
NM_001184721.1:c.482-128G>C NP_001171650.1:n.482-128G>C
NM_004130.3:c.482-128G>C NP_004121.2:n.482-128G>C
XM_017006275.1:c.305-128G>C XP_016861764.1:n.305-128G>C
XM_017006276.1:c.20-128G>C XP_016861765.1:n.20-128G>C
NM_004130.4:c.482-128G>C MANE Select NP_004121.2:n.482-128G>C
NM_001184720.2:c.482-128G>C NP_001171649.1:n.482-128G>C
NM_001184721.2:c.482-128G>C NP_001171650.1:n.482-128G>C