Canonical Allele Identifier: CA2340166096
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974716_48974717delinsAG , CM000681.2:g.48974716_48974717delinsAG GRCh38
NC_000019.9:g.49477973_49477974delinsAG , CM000681.1:g.49477973_49477974delinsAG GRCh37
NC_000019.8:g.54169785_54169786delinsAG NCBI36
NG_012923.1:g.23637_23638delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1325_1326delinsCT MANE Select ENSP00000317904.3:p.Pro442=
ENST00000263276.6:c.1133_1134delinsCT ENSP00000263276.6:p.Pro378=
ENST00000323798.7:c.1325_1326delinsCT ENSP00000317904.3:p.Pro442=
ENST00000472004.5:n.80_81delinsCT
ENST00000496048.1:n.232_233delinsCT
NM_001161587.1:c.1133_1134delinsCT NP_001155059.1:p.Pro378=
NM_002103.4:c.1325_1326delinsCT NP_002094.2:p.Pro442=
NR_027763.1:n.1384_1385delinsCT
NM_002103.5:c.1325_1326delinsCT MANE Select NP_002094.2:p.Pro442=
NM_001161587.2:c.1133_1134delinsCT NP_001155059.1:p.Pro378=
NR_027763.2:n.1340_1341delinsCT