Canonical Allele Identifier: CA2335088826
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38572936_38572971delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC , CM000681.2:g.38572936_38572971delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC GRCh38
NC_000019.9:g.39063576_39063611delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC , CM000681.1:g.39063576_39063611delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC GRCh37
NC_000019.8:g.43755416_43755451delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC NCBI36
NG_008866.1:g.144237_144272delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC , LRG_766:g.144237_144272delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.935-241_935-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC
ENST00000688602.1:c.2332-241_2332-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC
ENST00000689936.1:c.2304-241_2304-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC
ENST00000359596.8:c.13999-241_13999-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC MANE Select ENSP00000352608.2:n.13999-241_13999-206delinsACATTCCAGCCCTGAC...
ENST00000355481.8:c.13984-241_13984-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC ENSP00000347667.3:n.13984-241_13984-206delinsACATTCCAGCCCTGAC...
ENST00000359596.7:c.13999-241_13999-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC ENSP00000352608.2:n.13999-241_13999-206delinsACATTCCAGCCCTGAC...
ENST00000360985.7:c.13981-241_13981-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC ENSP00000354254.4:n.13981-241_13981-206delinsACATTCCAGCCCTGAC...
NM_000540.2:c.13999-241_13999-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC , LRG_766t1:c.13999-241_13999-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC NP_000531.2:n.13999-241_13999-206delinsACATTCCAGCCCTGACCCCCCT...
NM_001042723.1:c.13984-241_13984-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC NP_001036188.1:n.13984-241_13984-206delinsACATTCCAGCCCTGACCCC...
XM_006723317.1:c.13981-241_13981-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC XP_006723380.1:n.13981-241_13981-206delinsACATTCCAGCCCTGACCCC...
XM_006723319.1:c.13966-241_13966-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC XP_006723382.1:n.13966-241_13966-206delinsACATTCCAGCCCTGACCCC...
XM_011527204.1:c.13996-241_13996-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC XP_011525506.1:n.13996-241_13996-206delinsACATTCCAGCCCTGACCCC...
XM_011527205.1:c.13912-241_13912-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC XP_011525507.1:n.13912-241_13912-206delinsACATTCCAGCCCTGACCCC...
XM_006723317.2:c.13981-241_13981-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC XP_006723380.1:n.13981-241_13981-206delinsACATTCCAGCCCTGACCCC...
XM_006723319.2:c.13966-241_13966-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC XP_006723382.1:n.13966-241_13966-206delinsACATTCCAGCCCTGACCCC...
XM_011527205.2:c.13912-241_13912-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC XP_011525507.1:n.13912-241_13912-206delinsACATTCCAGCCCTGACCCC...
NM_000540.3:c.13999-241_13999-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC MANE Select NP_000531.2:n.13999-241_13999-206delinsACATTCCAGCCCTGACCCCCCT...
NM_001042723.2:c.13984-241_13984-206delinsACATTCCAGCCCTGACCCCCCTGCCTGTGCCTCCCC NP_001036188.1:n.13984-241_13984-206delinsACATTCCAGCCCTGACCCC...