Canonical Allele Identifier: CA2340166081
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974685A= , CM000681.2:g.48974685A= GRCh38
NC_000019.9:g.49477942A= , CM000681.1:g.49477942A= GRCh37
NC_000019.8:g.54169754A= NCBI36
NG_012923.1:g.23669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1357T= MANE Select ENSP00000317904.3:p.Ser453=
ENST00000263276.6:c.1165T= ENSP00000263276.6:p.Ser389=
ENST00000323798.7:c.1357T= ENSP00000317904.3:p.Ser453=
ENST00000472004.5:n.112T=
ENST00000496048.1:n.264T=
NM_001161587.1:c.1165T= NP_001155059.1:p.Ser389=
NM_002103.4:c.1357T= NP_002094.2:p.Ser453=
NR_027763.1:n.1416T=
NM_002103.5:c.1357T= MANE Select NP_002094.2:p.Ser453=
NM_001161587.2:c.1165T= NP_001155059.1:p.Ser389=
NR_027763.2:n.1372T=