Canonical Allele Identifier: CA2335054644

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38502799_38502820delinsAGGGGCAGGGGGAGGAGCAGGG , CM000681.2:g.38502799_38502820delinsAGGGGCAGGGGGAGGAGCAGGG	GRCh38
NC_000019.9:g.38993439_38993460delinsAGGGGCAGGGGGAGGAGCAGGG , CM000681.1:g.38993439_38993460delinsAGGGGCAGGGGGAGGAGCAGGG	GRCh37
NC_000019.8:g.43685279_43685300delinsAGGGGCAGGGGGAGGAGCAGGG	NCBI36
NG_008866.1:g.74100_74121delinsAGGGGCAGGGGGAGGAGCAGGG , LRG_766:g.74100_74121delinsAGGGGCAGGGGGAGGAGCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	ENSP00000471601.2:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAG...
ENST00000359596.8:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG MANE Select	ENSP00000352608.2:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAG...
ENST00000355481.8:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	ENSP00000347667.3:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAG...
ENST00000359596.7:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	ENSP00000352608.2:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAG...
ENST00000360985.7:c.7832+72_7833-60delinsAGGGGCAGGGGGAGGAGCAGGG	ENSP00000354254.4:n.7832+72_7833-60delinsAGGGGCAGGGGGAGGAGCAG...
ENST00000594335.5:c.1287+72_1288-60delinsAGGGGCAGGGGGAGGAGCAGGG
NM_000540.2:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG , LRG_766t1:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	NP_000531.2:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
NM_001042723.1:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	NP_001036188.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
XM_006723317.1:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	XP_006723380.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
XM_006723319.1:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	XP_006723382.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
XM_011527204.1:c.7832+72_7833-60delinsAGGGGCAGGGGGAGGAGCAGGG	XP_011525506.1:n.7832+72_7833-60delinsAGGGGCAGGGGGAGGAGCAGGG
XM_011527205.1:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	XP_011525507.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
XM_006723317.2:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	XP_006723380.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
XM_006723319.2:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	XP_006723382.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
XM_011527205.2:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	XP_011525507.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
XR_001753735.1:n.7918+72_7919-60delinsAGGGGCAGGGGGAGGAGCAGGG
NM_000540.3:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG MANE Select	NP_000531.2:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG
NM_001042723.2:c.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG	NP_001036188.1:n.7835+72_7836-60delinsAGGGGCAGGGGGAGGAGCAGGG