Canonical Allele Identifier: CA508081615

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477976G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974719G>C , CM000681.2:g.48974719G>C	GRCh38
NC_000019.9:g.49477976G>C , CM000681.1:g.49477976G>C	GRCh37
NC_000019.8:g.54169788G>C	NCBI36
NG_012923.1:g.23635C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1323C>G MANE Select	ENSP00000317904.3:p.Pro441=
ENST00000263276.6:c.1131C>G	ENSP00000263276.6:p.Pro377=
ENST00000323798.7:c.1323C>G	ENSP00000317904.3:p.Pro441=
ENST00000472004.5:n.78C>G
ENST00000496048.1:n.230C>G
NM_001161587.1:c.1131C>G	NP_001155059.1:p.Pro377=
NM_002103.4:c.1323C>G	NP_002094.2:p.Pro441=
NR_027763.1:n.1382C>G
NM_002103.5:c.1323C>G MANE Select	NP_002094.2:p.Pro441=
NM_001161587.2:c.1131C>G	NP_001155059.1:p.Pro377=
NR_027763.2:n.1338C>G