Canonical Allele Identifier: CA406761605

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477902A>C (hg19) ; chr19:g.48974645A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974645A>C , CM000681.2:g.48974645A>C	GRCh38
NC_000019.9:g.49477902A>C , CM000681.1:g.49477902A>C	GRCh37
NC_000019.8:g.54169714A>C	NCBI36
NG_012923.1:g.23709T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1397T>G MANE Select	ENSP00000317904.3:p.Phe466Cys
ENST00000263276.6:c.1205T>G	ENSP00000263276.6:p.Phe402Cys
ENST00000323798.7:c.1397T>G	ENSP00000317904.3:p.Phe466Cys
ENST00000472004.5:n.152T>G
ENST00000496048.1:n.304T>G
NM_001161587.1:c.1205T>G	NP_001155059.1:p.Phe402Cys
NM_002103.4:c.1397T>G	NP_002094.2:p.Phe466Cys
NR_027763.1:n.1456T>G
NM_002103.5:c.1397T>G MANE Select	NP_002094.2:p.Phe466Cys
NM_001161587.2:c.1205T>G	NP_001155059.1:p.Phe402Cys
NR_027763.2:n.1412T>G