Canonical Allele Identifier: CA406761740

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477966T>A (hg19) ; chr19:g.48974709T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1333A>T MANE Select	ENSP00000317904.3:p.Thr445Ser
ENST00000263276.6:c.1141A>T	ENSP00000263276.6:p.Thr381Ser
ENST00000323798.7:c.1333A>T	ENSP00000317904.3:p.Thr445Ser
ENST00000472004.5:n.88A>T
ENST00000496048.1:n.240A>T
NM_001161587.1:c.1141A>T	NP_001155059.1:p.Thr381Ser
NM_002103.4:c.1333A>T	NP_002094.2:p.Thr445Ser
NR_027763.1:n.1392A>T
NM_002103.5:c.1333A>T MANE Select	NP_002094.2:p.Thr445Ser
NM_001161587.2:c.1141A>T	NP_001155059.1:p.Thr381Ser
NR_027763.2:n.1348A>T