Canonical Allele Identifier: CA406761728

Gene: GYS1

Linked Data

• MyVariant Identifiers: chr19:g.49477960T>C (hg19) ; chr19:g.48974703T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974703T>C , CM000681.2:g.48974703T>C	GRCh38
NC_000019.9:g.49477960T>C , CM000681.1:g.49477960T>C	GRCh37
NC_000019.8:g.54169772T>C	NCBI36
NG_012923.1:g.23651A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1339A>G MANE Select	ENSP00000317904.3:p.Asn447Asp
ENST00000263276.6:c.1147A>G	ENSP00000263276.6:p.Asn383Asp
ENST00000323798.7:c.1339A>G	ENSP00000317904.3:p.Asn447Asp
ENST00000472004.5:n.94A>G
ENST00000496048.1:n.246A>G
NM_001161587.1:c.1147A>G	NP_001155059.1:p.Asn383Asp
NM_002103.4:c.1339A>G	NP_002094.2:p.Asn447Asp
NR_027763.1:n.1398A>G
NM_002103.5:c.1339A>G MANE Select	NP_002094.2:p.Asn447Asp
NM_001161587.2:c.1147A>G	NP_001155059.1:p.Asn383Asp
NR_027763.2:n.1354A>G