Canonical Allele Identifier: CA1410025482
Gene: GYG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148996150_148996152delinsAAT , CM000665.2:g.148996150_148996152delinsAAT GRCh38
NC_000003.11:g.148713937_148713939delinsAAT , CM000665.1:g.148713937_148713939delinsAAT GRCh37
NC_000003.10:g.150196627_150196629delinsAAT NCBI36
NG_027677.1:g.9743_9745delinsAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000345003.9:c.144-152_144-150delinsAAT MANE Select ENSP00000340736.4:n.144-152_144-150delinsAAT
ENST00000296048.10:c.144-152_144-150delinsAAT ENSP00000296048.6:n.144-152_144-150delinsAAT
ENST00000345003.8:c.144-152_144-150delinsAAT ENSP00000340736.4:n.144-152_144-150delinsAAT
ENST00000461191.1:c.144-152_144-150delinsAAT ENSP00000420247.1:n.144-152_144-150delinsAAT
ENST00000465547.1:n.50-165_50-163delinsAAT
ENST00000473005.1:c.6-152_6-150delinsAAT ENSP00000417671.1:n.6-152_6-150delinsAAT
ENST00000478067.1:n.245-152_245-150delinsAAT
ENST00000483267.5:c.144-152_144-150delinsAAT ENSP00000419499.1:n.144-152_144-150delinsAAT
ENST00000484197.5:c.144-152_144-150delinsAAT ENSP00000420683.1:n.144-152_144-150delinsAAT
ENST00000492285.6:c.6-152_6-150delinsAAT ENSP00000418297.2:n.6-152_6-150delinsAAT
ENST00000627418.2:c.144-152_144-150delinsAAT ENSP00000486061.1:n.144-152_144-150delinsAAT
NM_001184720.1:c.144-152_144-150delinsAAT NP_001171649.1:n.144-152_144-150delinsAAT
NM_001184721.1:c.144-152_144-150delinsAAT NP_001171650.1:n.144-152_144-150delinsAAT
NM_004130.3:c.144-152_144-150delinsAAT NP_004121.2:n.144-152_144-150delinsAAT
XM_017006275.1:c.-34-152_-34-150delinsAAT XP_016861764.1:n.-34-152_-34-150delinsAAT
NM_004130.4:c.144-152_144-150delinsAAT MANE Select NP_004121.2:n.144-152_144-150delinsAAT
NM_001184720.2:c.144-152_144-150delinsAAT NP_001171649.1:n.144-152_144-150delinsAAT
NM_001184721.2:c.144-152_144-150delinsAAT NP_001171650.1:n.144-152_144-150delinsAAT