Canonical Allele Identifier: CA406761741

Gene: GYS1

Linked Data

• dbSNP Id: rs2049625112
• MyVariant Identifiers: chr19:g.49477966T>C (hg19) ; chr19:g.48974709T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974709T>C , CM000681.2:g.48974709T>C	GRCh38
NC_000019.9:g.49477966T>C , CM000681.1:g.49477966T>C	GRCh37
NC_000019.8:g.54169778T>C	NCBI36
NG_012923.1:g.23645A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1333A>G MANE Select	ENSP00000317904.3:p.Thr445Ala
ENST00000263276.6:c.1141A>G	ENSP00000263276.6:p.Thr381Ala
ENST00000323798.7:c.1333A>G	ENSP00000317904.3:p.Thr445Ala
ENST00000472004.5:n.88A>G
ENST00000496048.1:n.240A>G
NM_001161587.1:c.1141A>G	NP_001155059.1:p.Thr381Ala
NM_002103.4:c.1333A>G	NP_002094.2:p.Thr445Ala
NR_027763.1:n.1392A>G
NM_002103.5:c.1333A>G MANE Select	NP_002094.2:p.Thr445Ala
NM_001161587.2:c.1141A>G	NP_001155059.1:p.Thr381Ala
NR_027763.2:n.1348A>G