Canonical Allele Identifier: CA406761745
Gene: GYS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974711C>G , CM000681.2:g.48974711C>G GRCh38
NC_000019.9:g.49477968C>G , CM000681.1:g.49477968C>G GRCh37
NC_000019.8:g.54169780C>G NCBI36
NG_012923.1:g.23643G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1331G>C MANE Select ENSP00000317904.3:p.Cys444Ser
ENST00000263276.6:c.1139G>C ENSP00000263276.6:p.Cys380Ser
ENST00000323798.7:c.1331G>C ENSP00000317904.3:p.Cys444Ser
ENST00000472004.5:n.86G>C
ENST00000496048.1:n.238G>C
NM_001161587.1:c.1139G>C NP_001155059.1:p.Cys380Ser
NM_002103.4:c.1331G>C NP_002094.2:p.Cys444Ser
NR_027763.1:n.1390G>C
NM_002103.5:c.1331G>C MANE Select NP_002094.2:p.Cys444Ser
NM_001161587.2:c.1139G>C NP_001155059.1:p.Cys380Ser
NR_027763.2:n.1346G>C