Canonical Allele Identifier: CA2340166099
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974720G= , CM000681.2:g.48974720G= GRCh38
NC_000019.9:g.49477977G= , CM000681.1:g.49477977G= GRCh37
NC_000019.8:g.54169789G= NCBI36
NG_012923.1:g.23634C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1322C= MANE Select ENSP00000317904.3:p.Pro441=
ENST00000263276.6:c.1130C= ENSP00000263276.6:p.Pro377=
ENST00000323798.7:c.1322C= ENSP00000317904.3:p.Pro441=
ENST00000472004.5:n.77C=
ENST00000496048.1:n.229C=
NM_001161587.1:c.1130C= NP_001155059.1:p.Pro377=
NM_002103.4:c.1322C= NP_002094.2:p.Pro441=
NR_027763.1:n.1381C=
NM_002103.5:c.1322C= MANE Select NP_002094.2:p.Pro441=
NM_001161587.2:c.1130C= NP_001155059.1:p.Pro377=
NR_027763.2:n.1337C=