Canonical Allele Identifier: CA2340166082
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974687G= , CM000681.2:g.48974687G= GRCh38
NC_000019.9:g.49477944G= , CM000681.1:g.49477944G= GRCh37
NC_000019.8:g.54169756G= NCBI36
NG_012923.1:g.23667C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1355C= MANE Select ENSP00000317904.3:p.Ser452=
ENST00000263276.6:c.1163C= ENSP00000263276.6:p.Ser388=
ENST00000323798.7:c.1355C= ENSP00000317904.3:p.Ser452=
ENST00000472004.5:n.110C=
ENST00000496048.1:n.262C=
NM_001161587.1:c.1163C= NP_001155059.1:p.Ser388=
NM_002103.4:c.1355C= NP_002094.2:p.Ser452=
NR_027763.1:n.1414C=
NM_002103.5:c.1355C= MANE Select NP_002094.2:p.Ser452=
NM_001161587.2:c.1163C= NP_001155059.1:p.Ser388=
NR_027763.2:n.1370C=