Canonical Allele Identifier: CA406761735
Gene: GYS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974706G>C , CM000681.2:g.48974706G>C GRCh38
NC_000019.9:g.49477963G>C , CM000681.1:g.49477963G>C GRCh37
NC_000019.8:g.54169775G>C NCBI36
NG_012923.1:g.23648C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1336C>G MANE Select ENSP00000317904.3:p.His446Asp
ENST00000263276.6:c.1144C>G ENSP00000263276.6:p.His382Asp
ENST00000323798.7:c.1336C>G ENSP00000317904.3:p.His446Asp
ENST00000472004.5:n.91C>G
ENST00000496048.1:n.243C>G
NM_001161587.1:c.1144C>G NP_001155059.1:p.His382Asp
NM_002103.4:c.1336C>G NP_002094.2:p.His446Asp
NR_027763.1:n.1395C>G
NM_002103.5:c.1336C>G MANE Select NP_002094.2:p.His446Asp
NM_001161587.2:c.1144C>G NP_001155059.1:p.His382Asp
NR_027763.2:n.1351C>G