Canonical Allele Identifier: CA508081611

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477970C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974713C>T , CM000681.2:g.48974713C>T	GRCh38
NC_000019.9:g.49477970C>T , CM000681.1:g.49477970C>T	GRCh37
NC_000019.8:g.54169782C>T	NCBI36
NG_012923.1:g.23641G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1329G>A MANE Select	ENSP00000317904.3:p.Val443=
ENST00000263276.6:c.1137G>A	ENSP00000263276.6:p.Val379=
ENST00000323798.7:c.1329G>A	ENSP00000317904.3:p.Val443=
ENST00000472004.5:n.84G>A
ENST00000496048.1:n.236G>A
NM_001161587.1:c.1137G>A	NP_001155059.1:p.Val379=
NM_002103.4:c.1329G>A	NP_002094.2:p.Val443=
NR_027763.1:n.1388G>A
NM_002103.5:c.1329G>A MANE Select	NP_002094.2:p.Val443=
NM_001161587.2:c.1137G>A	NP_001155059.1:p.Val379=
NR_027763.2:n.1344G>A