Canonical Allele Identifier: CA406761638

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477920A>C (hg19) ; chr19:g.48974663A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974663A>C , CM000681.2:g.48974663A>C	GRCh38
NC_000019.9:g.49477920A>C , CM000681.1:g.49477920A>C	GRCh37
NC_000019.8:g.54169732A>C	NCBI36
NG_012923.1:g.23691T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1379T>G MANE Select	ENSP00000317904.3:p.Ile460Ser
ENST00000263276.6:c.1187T>G	ENSP00000263276.6:p.Ile396Ser
ENST00000323798.7:c.1379T>G	ENSP00000317904.3:p.Ile460Ser
ENST00000472004.5:n.134T>G
ENST00000496048.1:n.286T>G
NM_001161587.1:c.1187T>G	NP_001155059.1:p.Ile396Ser
NM_002103.4:c.1379T>G	NP_002094.2:p.Ile460Ser
NR_027763.1:n.1438T>G
NM_002103.5:c.1379T>G MANE Select	NP_002094.2:p.Ile460Ser
NM_001161587.2:c.1187T>G	NP_001155059.1:p.Ile396Ser
NR_027763.2:n.1394T>G