Canonical Allele Identifier: CA2335054553

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38502769_38502784delinsAGGGGCAGGGGCAGGG , CM000681.2:g.38502769_38502784delinsAGGGGCAGGGGCAGGG	GRCh38
NC_000019.9:g.38993409_38993424delinsAGGGGCAGGGGCAGGG , CM000681.1:g.38993409_38993424delinsAGGGGCAGGGGCAGGG	GRCh37
NC_000019.8:g.43685249_43685264delinsAGGGGCAGGGGCAGGG	NCBI36
NG_008866.1:g.74070_74085delinsAGGGGCAGGGGCAGGG , LRG_766:g.74070_74085delinsAGGGGCAGGGGCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	ENSP00000471601.2:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
ENST00000359596.8:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG MANE Select	ENSP00000352608.2:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
ENST00000355481.8:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	ENSP00000347667.3:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
ENST00000359596.7:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	ENSP00000352608.2:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
ENST00000360985.7:c.7832+42_7832+57delinsAGGGGCAGGGGCAGGG	ENSP00000354254.4:n.7832+42_7832+57delinsAGGGGCAGGGGCAGGG
ENST00000594335.5:c.1287+42_1287+57delinsAGGGGCAGGGGCAGGG
NM_000540.2:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG , LRG_766t1:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	NP_000531.2:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
NM_001042723.1:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	NP_001036188.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
XM_006723317.1:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	XP_006723380.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
XM_006723319.1:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	XP_006723382.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
XM_011527204.1:c.7832+42_7832+57delinsAGGGGCAGGGGCAGGG	XP_011525506.1:n.7832+42_7832+57delinsAGGGGCAGGGGCAGGG
XM_011527205.1:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	XP_011525507.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
XM_006723317.2:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	XP_006723380.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
XM_006723319.2:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	XP_006723382.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
XM_011527205.2:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	XP_011525507.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
XR_001753735.1:n.7918+42_7918+57delinsAGGGGCAGGGGCAGGG
NM_000540.3:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG MANE Select	NP_000531.2:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG
NM_001042723.2:c.7835+42_7835+57delinsAGGGGCAGGGGCAGGG	NP_001036188.1:n.7835+42_7835+57delinsAGGGGCAGGGGCAGGG