Canonical Allele Identifier: CA2340166068
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974657C= , CM000681.2:g.48974657C= GRCh38
NC_000019.9:g.49477914C= , CM000681.1:g.49477914C= GRCh37
NC_000019.8:g.54169726C= NCBI36
NG_012923.1:g.23697G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1385G= MANE Select ENSP00000317904.3:p.Arg462=
ENST00000263276.6:c.1193G= ENSP00000263276.6:p.Arg398=
ENST00000323798.7:c.1385G= ENSP00000317904.3:p.Arg462=
ENST00000472004.5:n.140G=
ENST00000496048.1:n.292G=
NM_001161587.1:c.1193G= NP_001155059.1:p.Arg398=
NM_002103.4:c.1385G= NP_002094.2:p.Arg462=
NR_027763.1:n.1444G=
NM_002103.5:c.1385G= MANE Select NP_002094.2:p.Arg462=
NM_001161587.2:c.1193G= NP_001155059.1:p.Arg398=
NR_027763.2:n.1400G=