Canonical Allele Identifier: CA405688082
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580488G>C , CM000681.2:g.38580488G>C GRCh38
NC_000019.9:g.39071128G>C , CM000681.1:g.39071128G>C GRCh37
NC_000019.8:g.43762968G>C NCBI36
NG_008866.1:g.151789G>C , LRG_766:g.151789G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1566G>C
ENST00000688602.1:c.2963G>C
ENST00000689936.1:c.2935G>C
ENST00000359596.8:c.14630G>C MANE Select ENSP00000352608.2:p.Cys4877Ser
ENST00000355481.8:c.14615G>C ENSP00000347667.3:p.Cys4872Ser
ENST00000359596.7:c.14630G>C ENSP00000352608.2:p.Cys4877Ser
ENST00000360985.7:c.14612G>C ENSP00000354254.4:p.Cys4871Ser
NM_000540.2:c.14630G>C , LRG_766t1:c.14630G>C NP_000531.2:p.Cys4877Ser
NM_001042723.1:c.14615G>C NP_001036188.1:p.Cys4872Ser
XM_006723317.1:c.14612G>C XP_006723380.1:p.Cys4871Ser
XM_006723319.1:c.14597G>C XP_006723382.1:p.Cys4866Ser
XM_011527204.1:c.14627G>C XP_011525506.1:p.Cys4876Ser
XM_011527205.1:c.14543G>C XP_011525507.1:p.Cys4848Ser
XM_006723317.2:c.14612G>C XP_006723380.1:p.Cys4871Ser
XM_006723319.2:c.14597G>C XP_006723382.1:p.Cys4866Ser
XM_011527205.2:c.14543G>C XP_011525507.1:p.Cys4848Ser
NM_000540.3:c.14630G>C MANE Select NP_000531.2:p.Cys4877Ser
NM_001042723.2:c.14615G>C NP_001036188.1:p.Cys4872Ser