Canonical Allele Identifier: CA345413873
Gene: RYR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237784379A>T , CM000663.2:g.237784379A>T GRCh38
NC_000001.10:g.237947679A>T , CM000663.1:g.237947679A>T GRCh37
NC_000001.9:g.236014302A>T NCBI36
NG_008799.2:g.746978A>T
NG_008799.3:g.747196A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.*3759A>T ENSP00000499659.2:n.*3759A>T
ENST00000659194.3:c.12655A>T ENSP00000499653.3:p.Lys4219Ter
ENST00000660292.2:c.12688A>T ENSP00000499787.2:p.Lys4230Ter
ENST00000659194.2:c.4844A>T
ENST00000366574.7:c.12667A>T MANE Select ENSP00000355533.2:p.Lys4223Ter
ENST00000659194.1:c.4844A>T
ENST00000660292.1:c.2720A>T
ENST00000360064.7:c.12619A>T ENSP00000353174.7:p.Lys4207Ter
ENST00000366574.6:c.12667A>T ENSP00000355533.2:p.Lys4223Ter
ENST00000609119.1:n.3862A>T
NM_001035.2:c.12667A>T NP_001026.2:p.Lys4223Ter
XM_006711802.2:c.12721A>T XP_006711865.1:p.Lys4241Ter
XM_006711803.2:c.12718A>T XP_006711866.1:p.Lys4240Ter
XM_006711804.2:c.12697A>T XP_006711867.1:p.Lys4233Ter
XM_006711805.2:c.12691A>T XP_006711868.1:p.Lys4231Ter
XM_006711806.2:c.12685A>T XP_006711869.1:p.Lys4229Ter
XM_006711807.2:c.12661A>T XP_006711870.1:p.Lys4221Ter
XM_006711808.2:c.12484A>T XP_006711871.1:p.Lys4162Ter
XM_006711810.2:c.12628A>T XP_006711873.1:p.Lys4210Ter
XM_006711802.3:c.12721A>T XP_006711865.1:p.Lys4241Ter
XM_006711803.3:c.12718A>T XP_006711866.1:p.Lys4240Ter
XM_006711804.3:c.12697A>T XP_006711867.1:p.Lys4233Ter
XM_006711805.3:c.12691A>T XP_006711868.1:p.Lys4231Ter
XM_006711806.3:c.12685A>T XP_006711869.1:p.Lys4229Ter
XM_006711807.3:c.12661A>T XP_006711870.1:p.Lys4221Ter
XM_006711808.3:c.12484A>T XP_006711871.1:p.Lys4162Ter
XM_006711810.3:c.12628A>T XP_006711873.1:p.Lys4210Ter
XM_017002028.1:c.12700A>T XP_016857517.1:p.Lys4234Ter
NM_001035.3:c.12667A>T MANE Select NP_001026.2:p.Lys4223Ter