Canonical Allele Identifier: CA2335074449

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543663_38543676delinsAGGGCGCTCCCCCT , CM000681.2:g.38543663_38543676delinsAGGGCGCTCCCCCT	GRCh38
NC_000019.9:g.39034303_39034316delinsAGGGCGCTCCCCCT , CM000681.1:g.39034303_39034316delinsAGGGCGCTCCCCCT	GRCh37
NC_000019.8:g.43726143_43726156delinsAGGGCGCTCCCCCT	NCBI36
NG_008866.1:g.114964_114977delinsAGGGCGCTCCCCCT , LRG_766:g.114964_114977delinsAGGGCGCTCCCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.317+3_317+16delinsAGGGCGCTCCCCCT
ENST00000689936.1:c.299+3_299+16delinsAGGGCGCTCCCCCT
ENST00000359596.8:c.11907+3_11907+16delinsAGGGCGCTCCCCCT MANE Select	ENSP00000352608.2:n.11907+3_11907+16delinsAGGGCGCTCCCCCT
ENST00000355481.8:c.11892+3_11892+16delinsAGGGCGCTCCCCCT	ENSP00000347667.3:n.11892+3_11892+16delinsAGGGCGCTCCCCCT
ENST00000359596.7:c.11907+3_11907+16delinsAGGGCGCTCCCCCT	ENSP00000352608.2:n.11907+3_11907+16delinsAGGGCGCTCCCCCT
ENST00000360985.7:c.11889+3_11889+16delinsAGGGCGCTCCCCCT	ENSP00000354254.4:n.11889+3_11889+16delinsAGGGCGCTCCCCCT
ENST00000593322.1:c.516+3_516+16delinsAGGGCGCTCCCCCT
ENST00000594335.5:c.5276+3_5276+16delinsAGGGCGCTCCCCCT
NM_000540.2:c.11907+3_11907+16delinsAGGGCGCTCCCCCT , LRG_766t1:c.11907+3_11907+16delinsAGGGCGCTCCCCCT	NP_000531.2:n.11907+3_11907+16delinsAGGGCGCTCCCCCT
NM_001042723.1:c.11892+3_11892+16delinsAGGGCGCTCCCCCT	NP_001036188.1:n.11892+3_11892+16delinsAGGGCGCTCCCCCT
XM_006723317.1:c.11889+3_11889+16delinsAGGGCGCTCCCCCT	XP_006723380.1:n.11889+3_11889+16delinsAGGGCGCTCCCCCT
XM_006723319.1:c.11874+3_11874+16delinsAGGGCGCTCCCCCT	XP_006723382.1:n.11874+3_11874+16delinsAGGGCGCTCCCCCT
XM_011527204.1:c.11904+3_11904+16delinsAGGGCGCTCCCCCT	XP_011525506.1:n.11904+3_11904+16delinsAGGGCGCTCCCCCT
XM_011527205.1:c.11907+3_11907+16delinsAGGGCGCTCCCCCT	XP_011525507.1:n.11907+3_11907+16delinsAGGGCGCTCCCCCT
XM_006723317.2:c.11889+3_11889+16delinsAGGGCGCTCCCCCT	XP_006723380.1:n.11889+3_11889+16delinsAGGGCGCTCCCCCT
XM_006723319.2:c.11874+3_11874+16delinsAGGGCGCTCCCCCT	XP_006723382.1:n.11874+3_11874+16delinsAGGGCGCTCCCCCT
XM_011527205.2:c.11907+3_11907+16delinsAGGGCGCTCCCCCT	XP_011525507.1:n.11907+3_11907+16delinsAGGGCGCTCCCCCT
NM_000540.3:c.11907+3_11907+16delinsAGGGCGCTCCCCCT MANE Select	NP_000531.2:n.11907+3_11907+16delinsAGGGCGCTCCCCCT
NM_001042723.2:c.11892+3_11892+16delinsAGGGCGCTCCCCCT	NP_001036188.1:n.11892+3_11892+16delinsAGGGCGCTCCCCCT