Canonical Allele Identifier: CA405685017
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39068789T>G (hg19) chr19:g.38578149T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578149T>G , CM000681.2:g.38578149T>G GRCh38
NC_000019.9:g.39068789T>G , CM000681.1:g.39068789T>G GRCh37
NC_000019.8:g.43760629T>G NCBI36
NG_008866.1:g.149450T>G , LRG_766:g.149450T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1245T>G
ENST00000688602.1:c.2642T>G
ENST00000689936.1:c.2614T>G
ENST00000359596.8:c.14309T>G MANE Select ENSP00000352608.2:p.Met4770Arg
ENST00000355481.8:c.14294T>G ENSP00000347667.3:p.Met4765Arg
ENST00000359596.7:c.14309T>G ENSP00000352608.2:p.Met4770Arg
ENST00000360985.7:c.14291T>G ENSP00000354254.4:p.Met4764Arg
NM_000540.2:c.14309T>G , LRG_766t1:c.14309T>G NP_000531.2:p.Met4770Arg
NM_001042723.1:c.14294T>G NP_001036188.1:p.Met4765Arg
XM_006723317.1:c.14291T>G XP_006723380.1:p.Met4764Arg
XM_006723319.1:c.14276T>G XP_006723382.1:p.Met4759Arg
XM_011527204.1:c.14306T>G XP_011525506.1:p.Met4769Arg
XM_011527205.1:c.14222T>G XP_011525507.1:p.Met4741Arg
XM_006723317.2:c.14291T>G XP_006723380.1:p.Met4764Arg
XM_006723319.2:c.14276T>G XP_006723382.1:p.Met4759Arg
XM_011527205.2:c.14222T>G XP_011525507.1:p.Met4741Arg
NM_000540.3:c.14309T>G MANE Select NP_000531.2:p.Met4770Arg
NM_001042723.2:c.14294T>G NP_001036188.1:p.Met4765Arg
Search 100 bp 5'
Search 100 bp 3'