Canonical Allele Identifier: CA2335094657

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38584550_38584618delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC , CM000681.2:g.38584550_38584618delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	GRCh38
NC_000019.9:g.39075190_39075258delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC , CM000681.1:g.39075190_39075258delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	GRCh37
NC_000019.8:g.43767030_43767098delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	NCBI36
NG_008866.1:g.155851_155919delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC , LRG_766:g.155851_155919delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1583-393_1583-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC
ENST00000688602.1:c.2980-393_2980-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC
ENST00000689936.1:c.2952-393_2952-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC
ENST00000359596.8:c.14647-393_14647-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC MANE Select	ENSP00000352608.2:n.14647-393_14647-325delinsTATCCTGGCCCTGACC...
ENST00000355481.8:c.14632-393_14632-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	ENSP00000347667.3:n.14632-393_14632-325delinsTATCCTGGCCCTGACC...
ENST00000359596.7:c.14647-393_14647-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	ENSP00000352608.2:n.14647-393_14647-325delinsTATCCTGGCCCTGACC...
ENST00000360985.7:c.14629-393_14629-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	ENSP00000354254.4:n.14629-393_14629-325delinsTATCCTGGCCCTGACC...
NM_000540.2:c.14647-393_14647-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC , LRG_766t1:c.14647-393_14647-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	NP_000531.2:n.14647-393_14647-325delinsTATCCTGGCCCTGACCCCTCTG...
NM_001042723.1:c.14632-393_14632-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	NP_001036188.1:n.14632-393_14632-325delinsTATCCTGGCCCTGACCCCT...
XM_006723317.1:c.14629-393_14629-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	XP_006723380.1:n.14629-393_14629-325delinsTATCCTGGCCCTGACCCCT...
XM_006723319.1:c.14614-393_14614-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	XP_006723382.1:n.14614-393_14614-325delinsTATCCTGGCCCTGACCCCT...
XM_011527204.1:c.14644-393_14644-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	XP_011525506.1:n.14644-393_14644-325delinsTATCCTGGCCCTGACCCCT...
XM_011527205.1:c.14560-393_14560-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	XP_011525507.1:n.14560-393_14560-325delinsTATCCTGGCCCTGACCCCT...
XM_006723317.2:c.14629-393_14629-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	XP_006723380.1:n.14629-393_14629-325delinsTATCCTGGCCCTGACCCCT...
XM_006723319.2:c.14614-393_14614-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	XP_006723382.1:n.14614-393_14614-325delinsTATCCTGGCCCTGACCCCT...
XM_011527205.2:c.14560-393_14560-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	XP_011525507.1:n.14560-393_14560-325delinsTATCCTGGCCCTGACCCCT...
NM_000540.3:c.14647-393_14647-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC MANE Select	NP_000531.2:n.14647-393_14647-325delinsTATCCTGGCCCTGACCCCTCTG...
NM_001042723.2:c.14632-393_14632-325delinsTATCCTGGCCCTGACCCCTCTGCCTGTGCCCCCCTTATCCTGGCCCTGATTCCCCTGCCAGTGCCCCCC	NP_001036188.1:n.14632-393_14632-325delinsTATCCTGGCCCTGACCCCT...