Canonical Allele Identifier: CA2340166079
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974681T= , CM000681.2:g.48974681T= GRCh38
NC_000019.9:g.49477938T= , CM000681.1:g.49477938T= GRCh37
NC_000019.8:g.54169750T= NCBI36
NG_012923.1:g.23673A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1361A= MANE Select ENSP00000317904.3:p.Asp454=
ENST00000263276.6:c.1169A= ENSP00000263276.6:p.Asp390=
ENST00000323798.7:c.1361A= ENSP00000317904.3:p.Asp454=
ENST00000472004.5:n.116A=
ENST00000496048.1:n.268A=
NM_001161587.1:c.1169A= NP_001155059.1:p.Asp390=
NM_002103.4:c.1361A= NP_002094.2:p.Asp454=
NR_027763.1:n.1420A=
NM_002103.5:c.1361A= MANE Select NP_002094.2:p.Asp454=
NM_001161587.2:c.1169A= NP_001155059.1:p.Asp390=
NR_027763.2:n.1376A=