Canonical Allele Identifier: CA2335027003
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1972936980

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38446278dup , CM000681.2:g.38446278dup GRCh38
NC_000019.9:g.38936918dup , CM000681.1:g.38936918dup GRCh37
NC_000019.8:g.43628758dup NCBI36
NG_008866.1:g.17579dup , LRG_766:g.17579dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.632-194dup ENSP00000471601.2:n.632-194dup
ENST00000359596.8:c.632-194dup MANE Select ENSP00000352608.2:n.632-194dup
ENST00000355481.8:c.632-194dup ENSP00000347667.3:n.632-194dup
ENST00000359596.7:c.632-194dup ENSP00000352608.2:n.632-194dup
ENST00000360985.7:c.632-194dup ENSP00000354254.4:n.632-194dup
NM_000540.2:c.632-194dup , LRG_766t1:c.632-194dup NP_000531.2:n.632-194dup
NM_001042723.1:c.632-194dup NP_001036188.1:n.632-194dup
XM_006723317.1:c.632-194dup XP_006723380.1:n.632-194dup
XM_006723319.1:c.632-194dup XP_006723382.1:n.632-194dup
XM_011527204.1:c.632-194dup XP_011525506.1:n.632-194dup
XM_011527205.1:c.632-194dup XP_011525507.1:n.632-194dup
XM_006723317.2:c.632-194dup XP_006723380.1:n.632-194dup
XM_006723319.2:c.632-194dup XP_006723382.1:n.632-194dup
XM_011527205.2:c.632-194dup XP_011525507.1:n.632-194dup
XR_001753735.1:n.715-194dup
NM_000540.3:c.632-194dup MANE Select NP_000531.2:n.632-194dup
NM_001042723.2:c.632-194dup NP_001036188.1:n.632-194dup