Canonical Allele Identifier: CA2814348057
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38572322_38572327dup , CM000681.2:g.38572322_38572327dup GRCh38
NC_000019.9:g.39062962_39062967dup , CM000681.1:g.39062962_39062967dup GRCh37
NC_000019.8:g.43754802_43754807dup NCBI36
NG_008866.1:g.143623_143628dup , LRG_766:g.143623_143628dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.934+52_934+57dup
ENST00000688602.1:c.2331+52_2331+57dup
ENST00000689936.1:c.2303+52_2303+57dup
ENST00000359596.8:c.13998+52_13998+57dup MANE Select ENSP00000352608.2:n.13998+52_13998+57dup
ENST00000355481.8:c.13983+52_13983+57dup ENSP00000347667.3:n.13983+52_13983+57dup
ENST00000359596.7:c.13998+52_13998+57dup ENSP00000352608.2:n.13998+52_13998+57dup
ENST00000360985.7:c.13980+52_13980+57dup ENSP00000354254.4:n.13980+52_13980+57dup
NM_000540.2:c.13998+52_13998+57dup , LRG_766t1:c.13998+52_13998+57dup NP_000531.2:n.13998+52_13998+57dup
NM_001042723.1:c.13983+52_13983+57dup NP_001036188.1:n.13983+52_13983+57dup
XM_006723317.1:c.13980+52_13980+57dup XP_006723380.1:n.13980+52_13980+57dup
XM_006723319.1:c.13965+52_13965+57dup XP_006723382.1:n.13965+52_13965+57dup
XM_011527204.1:c.13995+52_13995+57dup XP_011525506.1:n.13995+52_13995+57dup
XM_011527205.1:c.13911+52_13911+57dup XP_011525507.1:n.13911+52_13911+57dup
XM_006723317.2:c.13980+52_13980+57dup XP_006723380.1:n.13980+52_13980+57dup
XM_006723319.2:c.13965+52_13965+57dup XP_006723382.1:n.13965+52_13965+57dup
XM_011527205.2:c.13911+52_13911+57dup XP_011525507.1:n.13911+52_13911+57dup
NM_000540.3:c.13998+52_13998+57dup MANE Select NP_000531.2:n.13998+52_13998+57dup
NM_001042723.2:c.13983+52_13983+57dup NP_001036188.1:n.13983+52_13983+57dup