Canonical Allele Identifier: CA2340166093
Gene: GYS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974715_48974716delinsCA , CM000681.2:g.48974715_48974716delinsCA GRCh38
NC_000019.9:g.49477972_49477973delinsCA , CM000681.1:g.49477972_49477973delinsCA GRCh37
NC_000019.8:g.54169784_54169785delinsCA NCBI36
NG_012923.1:g.23638_23639delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1326_1327delinsTG MANE Select ENSP00000317904.3:p.Pro442=
ENST00000263276.6:c.1134_1135delinsTG ENSP00000263276.6:p.Pro378=
ENST00000323798.7:c.1326_1327delinsTG ENSP00000317904.3:p.Pro442=
ENST00000472004.5:n.81_82delinsTG
ENST00000496048.1:n.233_234delinsTG
NM_001161587.1:c.1134_1135delinsTG NP_001155059.1:p.Pro378=
NM_002103.4:c.1326_1327delinsTG NP_002094.2:p.Pro442=
NR_027763.1:n.1385_1386delinsTG
NM_002103.5:c.1326_1327delinsTG MANE Select NP_002094.2:p.Pro442=
NM_001161587.2:c.1134_1135delinsTG NP_001155059.1:p.Pro378=
NR_027763.2:n.1341_1342delinsTG