Canonical Allele Identifier: CA405682395

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063892C>T (hg19) ; chr19:g.38573252C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573252C>T , CM000681.2:g.38573252C>T	GRCh38
NC_000019.9:g.39063892C>T , CM000681.1:g.39063892C>T	GRCh37
NC_000019.8:g.43755732C>T	NCBI36
NG_008866.1:g.144553C>T , LRG_766:g.144553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1010C>T
ENST00000688602.1:c.2407C>T
ENST00000689936.1:c.2379C>T
ENST00000359596.8:c.14074C>T MANE Select	ENSP00000352608.2:p.Gln4692Ter
ENST00000355481.8:c.14059C>T	ENSP00000347667.3:p.Gln4687Ter
ENST00000359596.7:c.14074C>T	ENSP00000352608.2:p.Gln4692Ter
ENST00000360985.7:c.14056C>T	ENSP00000354254.4:p.Gln4686Ter
NM_000540.2:c.14074C>T , LRG_766t1:c.14074C>T	NP_000531.2:p.Gln4692Ter
NM_001042723.1:c.14059C>T	NP_001036188.1:p.Gln4687Ter
XM_006723317.1:c.14056C>T	XP_006723380.1:p.Gln4686Ter
XM_006723319.1:c.14041C>T	XP_006723382.1:p.Gln4681Ter
XM_011527204.1:c.14071C>T	XP_011525506.1:p.Gln4691Ter
XM_011527205.1:c.13987C>T	XP_011525507.1:p.Gln4663Ter
XM_006723317.2:c.14056C>T	XP_006723380.1:p.Gln4686Ter
XM_006723319.2:c.14041C>T	XP_006723382.1:p.Gln4681Ter
XM_011527205.2:c.13987C>T	XP_011525507.1:p.Gln4663Ter
NM_000540.3:c.14074C>T MANE Select	NP_000531.2:p.Gln4692Ter
NM_001042723.2:c.14059C>T	NP_001036188.1:p.Gln4687Ter