Canonical Allele Identifier: CA2340166095
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974716A= , CM000681.2:g.48974716A= GRCh38
NC_000019.9:g.49477973A= , CM000681.1:g.49477973A= GRCh37
NC_000019.8:g.54169785A= NCBI36
NG_012923.1:g.23638T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1326T= MANE Select ENSP00000317904.3:p.Pro442=
ENST00000263276.6:c.1134T= ENSP00000263276.6:p.Pro378=
ENST00000323798.7:c.1326T= ENSP00000317904.3:p.Pro442=
ENST00000472004.5:n.81T=
ENST00000496048.1:n.233T=
NM_001161587.1:c.1134T= NP_001155059.1:p.Pro378=
NM_002103.4:c.1326T= NP_002094.2:p.Pro442=
NR_027763.1:n.1385T=
NM_002103.5:c.1326T= MANE Select NP_002094.2:p.Pro442=
NM_001161587.2:c.1134T= NP_001155059.1:p.Pro378=
NR_027763.2:n.1341T=