Canonical Allele Identifier: CA354909950
Gene: GYG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148994210C>A , CM000665.2:g.148994210C>A GRCh38
NC_000003.11:g.148711997C>A , CM000665.1:g.148711997C>A GRCh37
NC_000003.10:g.150194687C>A NCBI36
NG_027677.1:g.7803C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345003.9:c.76C>A MANE Select ENSP00000340736.4:p.Leu26Met
ENST00000296048.10:c.76C>A ENSP00000296048.6:p.Leu26Met
ENST00000345003.8:c.76C>A ENSP00000340736.4:p.Leu26Met
ENST00000461191.1:c.76C>A ENSP00000420247.1:p.Leu26Met
ENST00000473005.1:c.-63C>A ENSP00000417671.1:n.-63C>A
ENST00000478067.1:n.177C>A
ENST00000483267.5:c.76C>A ENSP00000419499.1:p.Leu26Met
ENST00000484197.5:c.76C>A ENSP00000420683.1:p.Leu26Met
ENST00000492285.6:c.-63C>A ENSP00000418297.2:n.-63C>A
ENST00000627418.2:c.76C>A ENSP00000486061.1:p.Leu26Met
NM_001184720.1:c.76C>A NP_001171649.1:p.Leu26Met
NM_001184721.1:c.76C>A NP_001171650.1:p.Leu26Met
NM_004130.3:c.76C>A NP_004121.2:p.Leu26Met
XM_017006275.1:c.-34-2092C>A XP_016861764.1:n.-34-2092C>A
NM_004130.4:c.76C>A MANE Select NP_004121.2:p.Leu26Met
NM_001184720.2:c.76C>A NP_001171649.1:p.Leu26Met
NM_001184721.2:c.76C>A NP_001171650.1:p.Leu26Met