Canonical Allele Identifier: CA2340166085
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974692A= , CM000681.2:g.48974692A= GRCh38
NC_000019.9:g.49477949A= , CM000681.1:g.49477949A= GRCh37
NC_000019.8:g.54169761A= NCBI36
NG_012923.1:g.23662T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1350T= MANE Select ENSP00000317904.3:p.Asp450=
ENST00000263276.6:c.1158T= ENSP00000263276.6:p.Asp386=
ENST00000323798.7:c.1350T= ENSP00000317904.3:p.Asp450=
ENST00000472004.5:n.105T=
ENST00000496048.1:n.257T=
NM_001161587.1:c.1158T= NP_001155059.1:p.Asp386=
NM_002103.4:c.1350T= NP_002094.2:p.Asp450=
NR_027763.1:n.1409T=
NM_002103.5:c.1350T= MANE Select NP_002094.2:p.Asp450=
NM_001161587.2:c.1158T= NP_001155059.1:p.Asp386=
NR_027763.2:n.1365T=