Canonical Allele Identifier: CA405692920

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39076768T>G (hg19) ; chr19:g.38586128T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38586128T>G , CM000681.2:g.38586128T>G	GRCh38
NC_000019.9:g.39076768T>G , CM000681.1:g.39076768T>G	GRCh37
NC_000019.8:g.43768608T>G	NCBI36
NG_008866.1:g.157429T>G , LRG_766:g.157429T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1842T>G
ENST00000688602.1:c.3239T>G
ENST00000689936.1:c.3211T>G
ENST00000692547.1:n.299T>G
ENST00000359596.8:c.14906T>G MANE Select	ENSP00000352608.2:p.Phe4969Cys
ENST00000355481.8:c.14891T>G	ENSP00000347667.3:p.Phe4964Cys
ENST00000359596.7:c.14906T>G	ENSP00000352608.2:p.Phe4969Cys
ENST00000360985.7:c.14888T>G	ENSP00000354254.4:p.Phe4963Cys
NM_000540.2:c.14906T>G , LRG_766t1:c.14906T>G	NP_000531.2:p.Phe4969Cys
NM_001042723.1:c.14891T>G	NP_001036188.1:p.Phe4964Cys
XM_006723317.1:c.14888T>G	XP_006723380.1:p.Phe4963Cys
XM_006723319.1:c.14873T>G	XP_006723382.1:p.Phe4958Cys
XM_011527204.1:c.14903T>G	XP_011525506.1:p.Phe4968Cys
XM_011527205.1:c.14819T>G	XP_011525507.1:p.Phe4940Cys
XM_006723317.2:c.14888T>G	XP_006723380.1:p.Phe4963Cys
XM_006723319.2:c.14873T>G	XP_006723382.1:p.Phe4958Cys
XM_011527205.2:c.14819T>G	XP_011525507.1:p.Phe4940Cys
NM_000540.3:c.14906T>G MANE Select	NP_000531.2:p.Phe4969Cys
NM_001042723.2:c.14891T>G	NP_001036188.1:p.Phe4964Cys