Canonical Allele Identifier: CA405687552
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580371T>G , CM000681.2:g.38580371T>G GRCh38
NC_000019.9:g.39071011T>G , CM000681.1:g.39071011T>G GRCh37
NC_000019.8:g.43762851T>G NCBI36
NG_008866.1:g.151672T>G , LRG_766:g.151672T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1449T>G
ENST00000688602.1:c.2846T>G
ENST00000689936.1:c.2818T>G
ENST00000359596.8:c.14513T>G MANE Select ENSP00000352608.2:p.Leu4838Arg
ENST00000355481.8:c.14498T>G ENSP00000347667.3:p.Leu4833Arg
ENST00000359596.7:c.14513T>G ENSP00000352608.2:p.Leu4838Arg
ENST00000360985.7:c.14495T>G ENSP00000354254.4:p.Leu4832Arg
NM_000540.2:c.14513T>G , LRG_766t1:c.14513T>G NP_000531.2:p.Leu4838Arg
NM_001042723.1:c.14498T>G NP_001036188.1:p.Leu4833Arg
XM_006723317.1:c.14495T>G XP_006723380.1:p.Leu4832Arg
XM_006723319.1:c.14480T>G XP_006723382.1:p.Leu4827Arg
XM_011527204.1:c.14510T>G XP_011525506.1:p.Leu4837Arg
XM_011527205.1:c.14426T>G XP_011525507.1:p.Leu4809Arg
XM_006723317.2:c.14495T>G XP_006723380.1:p.Leu4832Arg
XM_006723319.2:c.14480T>G XP_006723382.1:p.Leu4827Arg
XM_011527205.2:c.14426T>G XP_011525507.1:p.Leu4809Arg
NM_000540.3:c.14513T>G MANE Select NP_000531.2:p.Leu4838Arg
NM_001042723.2:c.14498T>G NP_001036188.1:p.Leu4833Arg