Canonical Allele Identifier: CA508081601

Gene: GYS1

Linked Data

• dbSNP Id: rs2038617390
• MyVariant Identifiers: chr19:g.49477946G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974689G>A , CM000681.2:g.48974689G>A	GRCh38
NC_000019.9:g.49477946G>A , CM000681.1:g.49477946G>A	GRCh37
NC_000019.8:g.54169758G>A	NCBI36
NG_012923.1:g.23665C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1353C>T MANE Select	ENSP00000317904.3:p.Asp451=
ENST00000263276.6:c.1161C>T	ENSP00000263276.6:p.Asp387=
ENST00000323798.7:c.1353C>T	ENSP00000317904.3:p.Asp451=
ENST00000472004.5:n.108C>T
ENST00000496048.1:n.260C>T
NM_001161587.1:c.1161C>T	NP_001155059.1:p.Asp387=
NM_002103.4:c.1353C>T	NP_002094.2:p.Asp451=
NR_027763.1:n.1412C>T
NM_002103.5:c.1353C>T MANE Select	NP_002094.2:p.Asp451=
NM_001161587.2:c.1161C>T	NP_001155059.1:p.Asp387=
NR_027763.2:n.1368C>T