Canonical Allele Identifier: CA2340166088
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974704G= , CM000681.2:g.48974704G= GRCh38
NC_000019.9:g.49477961G= , CM000681.1:g.49477961G= GRCh37
NC_000019.8:g.54169773G= NCBI36
NG_012923.1:g.23650C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1338C= MANE Select ENSP00000317904.3:p.His446=
ENST00000263276.6:c.1146C= ENSP00000263276.6:p.His382=
ENST00000323798.7:c.1338C= ENSP00000317904.3:p.His446=
ENST00000472004.5:n.93C=
ENST00000496048.1:n.245C=
NM_001161587.1:c.1146C= NP_001155059.1:p.His382=
NM_002103.4:c.1338C= NP_002094.2:p.His446=
NR_027763.1:n.1397C=
NM_002103.5:c.1338C= MANE Select NP_002094.2:p.His446=
NM_001161587.2:c.1146C= NP_001155059.1:p.His382=
NR_027763.2:n.1353C=