Canonical Allele Identifier: CA1410022580
Gene: GYG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148994119_148994121delinsGTT , CM000665.2:g.148994119_148994121delinsGTT GRCh38
NC_000003.11:g.148711906_148711908delinsGTT , CM000665.1:g.148711906_148711908delinsGTT GRCh37
NC_000003.10:g.150194596_150194598delinsGTT NCBI36
NG_027677.1:g.7712_7714delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000345003.9:c.8-23_8-21delinsGTT MANE Select ENSP00000340736.4:n.8-23_8-21delinsGTT
ENST00000296048.10:c.8-23_8-21delinsGTT ENSP00000296048.6:n.8-23_8-21delinsGTT
ENST00000345003.8:c.8-23_8-21delinsGTT ENSP00000340736.4:n.8-23_8-21delinsGTT
ENST00000461191.1:c.8-23_8-21delinsGTT ENSP00000420247.1:n.8-23_8-21delinsGTT
ENST00000473005.1:c.-131-23_-131-21delinsGTT ENSP00000417671.1:n.-131-23_-131-21delinsGTT
ENST00000478067.1:n.109-23_109-21delinsGTT
ENST00000483267.5:c.8-23_8-21delinsGTT ENSP00000419499.1:n.8-23_8-21delinsGTT
ENST00000484197.5:c.8-23_8-21delinsGTT ENSP00000420683.1:n.8-23_8-21delinsGTT
ENST00000492285.6:c.-131-23_-131-21delinsGTT ENSP00000418297.2:n.-131-23_-131-21delinsGTT
ENST00000627418.2:c.8-23_8-21delinsGTT ENSP00000486061.1:n.8-23_8-21delinsGTT
NM_001184720.1:c.8-23_8-21delinsGTT NP_001171649.1:n.8-23_8-21delinsGTT
NM_001184721.1:c.8-23_8-21delinsGTT NP_001171650.1:n.8-23_8-21delinsGTT
NM_004130.3:c.8-23_8-21delinsGTT NP_004121.2:n.8-23_8-21delinsGTT
XM_017006275.1:c.-34-2183_-34-2181delinsGTT XP_016861764.1:n.-34-2183_-34-2181delinsGTT
NM_004130.4:c.8-23_8-21delinsGTT MANE Select NP_004121.2:n.8-23_8-21delinsGTT
NM_001184720.2:c.8-23_8-21delinsGTT NP_001171649.1:n.8-23_8-21delinsGTT
NM_001184721.2:c.8-23_8-21delinsGTT NP_001171650.1:n.8-23_8-21delinsGTT