Canonical Allele Identifier: CA405687877
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580454A>T , CM000681.2:g.38580454A>T GRCh38
NC_000019.9:g.39071094A>T , CM000681.1:g.39071094A>T GRCh37
NC_000019.8:g.43762934A>T NCBI36
NG_008866.1:g.151755A>T , LRG_766:g.151755A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1532A>T
ENST00000688602.1:c.2929A>T
ENST00000689936.1:c.2901A>T
ENST00000359596.8:c.14596A>T MANE Select ENSP00000352608.2:p.Lys4866Ter
ENST00000355481.8:c.14581A>T ENSP00000347667.3:p.Lys4861Ter
ENST00000359596.7:c.14596A>T ENSP00000352608.2:p.Lys4866Ter
ENST00000360985.7:c.14578A>T ENSP00000354254.4:p.Lys4860Ter
NM_000540.2:c.14596A>T , LRG_766t1:c.14596A>T NP_000531.2:p.Lys4866Ter
NM_001042723.1:c.14581A>T NP_001036188.1:p.Lys4861Ter
XM_006723317.1:c.14578A>T XP_006723380.1:p.Lys4860Ter
XM_006723319.1:c.14563A>T XP_006723382.1:p.Lys4855Ter
XM_011527204.1:c.14593A>T XP_011525506.1:p.Lys4865Ter
XM_011527205.1:c.14509A>T XP_011525507.1:p.Lys4837Ter
XM_006723317.2:c.14578A>T XP_006723380.1:p.Lys4860Ter
XM_006723319.2:c.14563A>T XP_006723382.1:p.Lys4855Ter
XM_011527205.2:c.14509A>T XP_011525507.1:p.Lys4837Ter
NM_000540.3:c.14596A>T MANE Select NP_000531.2:p.Lys4866Ter
NM_001042723.2:c.14581A>T NP_001036188.1:p.Lys4861Ter