Canonical Allele Identifier: CA406761698

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477948C>A (hg19) ; chr19:g.48974691C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974691C>A , CM000681.2:g.48974691C>A	GRCh38
NC_000019.9:g.49477948C>A , CM000681.1:g.49477948C>A	GRCh37
NC_000019.8:g.54169760C>A	NCBI36
NG_012923.1:g.23663G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1351G>T MANE Select	ENSP00000317904.3:p.Asp451Tyr
ENST00000263276.6:c.1159G>T	ENSP00000263276.6:p.Asp387Tyr
ENST00000323798.7:c.1351G>T	ENSP00000317904.3:p.Asp451Tyr
ENST00000472004.5:n.106G>T
ENST00000496048.1:n.258G>T
NM_001161587.1:c.1159G>T	NP_001155059.1:p.Asp387Tyr
NM_002103.4:c.1351G>T	NP_002094.2:p.Asp451Tyr
NR_027763.1:n.1410G>T
NM_002103.5:c.1351G>T MANE Select	NP_002094.2:p.Asp451Tyr
NM_001161587.2:c.1159G>T	NP_001155059.1:p.Asp387Tyr
NR_027763.2:n.1366G>T