Canonical Allele Identifier: CA2335092448
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580382G= , CM000681.2:g.38580382G= GRCh38
NC_000019.9:g.39071022G= , CM000681.1:g.39071022G= GRCh37
NC_000019.8:g.43762862G= NCBI36
NG_008866.1:g.151683G= , LRG_766:g.151683G=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1460G=
ENST00000688602.1:c.2857G=
ENST00000689936.1:c.2829G=
ENST00000359596.8:c.14524G= MANE Select ENSP00000352608.2:p.Val4842=
ENST00000355481.8:c.14509G= ENSP00000347667.3:p.Val4837=
ENST00000359596.7:c.14524G= ENSP00000352608.2:p.Val4842=
ENST00000360985.7:c.14506G= ENSP00000354254.4:p.Val4836=
NM_000540.2:c.14524G= , LRG_766t1:c.14524G= NP_000531.2:p.Val4842=
NM_001042723.1:c.14509G= NP_001036188.1:p.Val4837=
XM_006723317.1:c.14506G= XP_006723380.1:p.Val4836=
XM_006723319.1:c.14491G= XP_006723382.1:p.Val4831=
XM_011527204.1:c.14521G= XP_011525506.1:p.Val4841=
XM_011527205.1:c.14437G= XP_011525507.1:p.Val4813=
XM_006723317.2:c.14506G= XP_006723380.1:p.Val4836=
XM_006723319.2:c.14491G= XP_006723382.1:p.Val4831=
XM_011527205.2:c.14437G= XP_011525507.1:p.Val4813=
NM_000540.3:c.14524G= MANE Select NP_000531.2:p.Val4842=
NM_001042723.2:c.14509G= NP_001036188.1:p.Val4837=