Canonical Allele Identifier: CA2335091301
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577977G= , CM000681.2:g.38577977G= GRCh38
NC_000019.9:g.39068617G= , CM000681.1:g.39068617G= GRCh37
NC_000019.8:g.43760457G= NCBI36
NG_008866.1:g.149278G= , LRG_766:g.149278G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1168G=
ENST00000688602.1:c.2565G=
ENST00000689936.1:c.2537G=
ENST00000359596.8:c.14232G= MANE Select ENSP00000352608.2:p.Met4744=
ENST00000355481.8:c.14217G= ENSP00000347667.3:p.Met4739=
ENST00000359596.7:c.14232G= ENSP00000352608.2:p.Met4744=
ENST00000360985.7:c.14214G= ENSP00000354254.4:p.Met4738=
NM_000540.2:c.14232G= , LRG_766t1:c.14232G= NP_000531.2:p.Met4744=
NM_001042723.1:c.14217G= NP_001036188.1:p.Met4739=
XM_006723317.1:c.14214G= XP_006723380.1:p.Met4738=
XM_006723319.1:c.14199G= XP_006723382.1:p.Met4733=
XM_011527204.1:c.14229G= XP_011525506.1:p.Met4743=
XM_011527205.1:c.14145G= XP_011525507.1:p.Met4715=
XM_006723317.2:c.14214G= XP_006723380.1:p.Met4738=
XM_006723319.2:c.14199G= XP_006723382.1:p.Met4733=
XM_011527205.2:c.14145G= XP_011525507.1:p.Met4715=
NM_000540.3:c.14232G= MANE Select NP_000531.2:p.Met4744=
NM_001042723.2:c.14217G= NP_001036188.1:p.Met4739=