Canonical Allele Identifier: CA405687672

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071048C>G (hg19) ; chr19:g.38580408C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580408C>G , CM000681.2:g.38580408C>G	GRCh38
NC_000019.9:g.39071048C>G , CM000681.1:g.39071048C>G	GRCh37
NC_000019.8:g.43762888C>G	NCBI36
NG_008866.1:g.151709C>G , LRG_766:g.151709C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1486C>G
ENST00000688602.1:c.2883C>G
ENST00000689936.1:c.2855C>G
ENST00000359596.8:c.14550C>G MANE Select	ENSP00000352608.2:p.Tyr4850Ter
ENST00000355481.8:c.14535C>G	ENSP00000347667.3:p.Tyr4845Ter
ENST00000359596.7:c.14550C>G	ENSP00000352608.2:p.Tyr4850Ter
ENST00000360985.7:c.14532C>G	ENSP00000354254.4:p.Tyr4844Ter
NM_000540.2:c.14550C>G , LRG_766t1:c.14550C>G	NP_000531.2:p.Tyr4850Ter
NM_001042723.1:c.14535C>G	NP_001036188.1:p.Tyr4845Ter
XM_006723317.1:c.14532C>G	XP_006723380.1:p.Tyr4844Ter
XM_006723319.1:c.14517C>G	XP_006723382.1:p.Tyr4839Ter
XM_011527204.1:c.14547C>G	XP_011525506.1:p.Tyr4849Ter
XM_011527205.1:c.14463C>G	XP_011525507.1:p.Tyr4821Ter
XM_006723317.2:c.14532C>G	XP_006723380.1:p.Tyr4844Ter
XM_006723319.2:c.14517C>G	XP_006723382.1:p.Tyr4839Ter
XM_011527205.2:c.14463C>G	XP_011525507.1:p.Tyr4821Ter
NM_000540.3:c.14550C>G MANE Select	NP_000531.2:p.Tyr4850Ter
NM_001042723.2:c.14535C>G	NP_001036188.1:p.Tyr4845Ter