Canonical Allele Identifier: CA2586290323
Gene: GYS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48974580C>G , CM000681.2:g.48974580C>G GRCh38
NC_000019.9:g.49477837C>G , CM000681.1:g.49477837C>G GRCh37
NC_000019.8:g.54169649C>G NCBI36
NG_012923.1:g.23774G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323798.8:c.1422+40G>C MANE Select ENSP00000317904.3:n.1422+40G>C
ENST00000263276.6:c.1230+40G>C ENSP00000263276.6:n.1230+40G>C
ENST00000323798.7:c.1422+40G>C ENSP00000317904.3:n.1422+40G>C
ENST00000472004.5:n.177+40G>C
ENST00000496048.1:n.329+40G>C
NM_001161587.1:c.1230+40G>C NP_001155059.1:n.1230+40G>C
NM_002103.4:c.1422+40G>C NP_002094.2:n.1422+40G>C
NR_027763.1:n.1481+40G>C
NM_002103.5:c.1422+40G>C MANE Select NP_002094.2:n.1422+40G>C
NM_001161587.2:c.1230+40G>C NP_001155059.1:n.1230+40G>C
NR_027763.2:n.1437+40G>C