Canonical Allele Identifier: CA406761676

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477938T>C (hg19) ; chr19:g.48974681T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974681T>C , CM000681.2:g.48974681T>C	GRCh38
NC_000019.9:g.49477938T>C , CM000681.1:g.49477938T>C	GRCh37
NC_000019.8:g.54169750T>C	NCBI36
NG_012923.1:g.23673A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1361A>G MANE Select	ENSP00000317904.3:p.Asp454Gly
ENST00000263276.6:c.1169A>G	ENSP00000263276.6:p.Asp390Gly
ENST00000323798.7:c.1361A>G	ENSP00000317904.3:p.Asp454Gly
ENST00000472004.5:n.116A>G
ENST00000496048.1:n.268A>G
NM_001161587.1:c.1169A>G	NP_001155059.1:p.Asp390Gly
NM_002103.4:c.1361A>G	NP_002094.2:p.Asp454Gly
NR_027763.1:n.1420A>G
NM_002103.5:c.1361A>G MANE Select	NP_002094.2:p.Asp454Gly
NM_001161587.2:c.1169A>G	NP_001155059.1:p.Asp390Gly
NR_027763.2:n.1376A>G