Canonical Allele Identifier: CA2335094906
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1974399396

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38584912_38584913insCC , CM000681.2:g.38584912_38584913insCC GRCh38
NC_000019.9:g.39075552_39075553insCC , CM000681.1:g.39075552_39075553insCC GRCh37
NC_000019.8:g.43767392_43767393insCC NCBI36
NG_008866.1:g.156213_156214insCC , LRG_766:g.156213_156214insCC

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1583-31_1583-30insCC
ENST00000688602.1:c.2980-31_2980-30insCC
ENST00000689936.1:c.2952-31_2952-30insCC
ENST00000692547.1:n.9_10insCC
ENST00000359596.8:c.14647-31_14647-30insCC MANE Select ENSP00000352608.2:n.14647-31_14647-30insC...
ENST00000355481.8:c.14632-31_14632-30insCC ENSP00000347667.3:n.14632-31_14632-30insC...
ENST00000359596.7:c.14647-31_14647-30insCC ENSP00000352608.2:n.14647-31_14647-30insC...
ENST00000360985.7:c.14629-31_14629-30insCC ENSP00000354254.4:n.14629-31_14629-30insC...
NM_000540.2:c.14647-31_14647-30insCC , LRG_766t1:c.14647-31_14647-30insCC NP_000531.2:n.14647-31_14647-30insCC
NM_001042723.1:c.14632-31_14632-30insCC NP_001036188.1:n.14632-31_14632-30insCC
XM_006723317.1:c.14629-31_14629-30insCC XP_006723380.1:n.14629-31_14629-30insCC
XM_006723319.1:c.14614-31_14614-30insCC XP_006723382.1:n.14614-31_14614-30insCC
XM_011527204.1:c.14644-31_14644-30insCC XP_011525506.1:n.14644-31_14644-30insCC
XM_011527205.1:c.14560-31_14560-30insCC XP_011525507.1:n.14560-31_14560-30insCC
XM_006723317.2:c.14629-31_14629-30insCC XP_006723380.1:n.14629-31_14629-30insCC
XM_006723319.2:c.14614-31_14614-30insCC XP_006723382.1:n.14614-31_14614-30insCC
XM_011527205.2:c.14560-31_14560-30insCC XP_011525507.1:n.14560-31_14560-30insCC
NM_000540.3:c.14647-31_14647-30insCC MANE Select NP_000531.2:n.14647-31_14647-30insCC
NM_001042723.2:c.14632-31_14632-30insCC NP_001036188.1:n.14632-31_14632-30insCC