Canonical Allele Identifier: CA345413498
Gene: RYR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237784218A>G , CM000663.2:g.237784218A>G GRCh38
NC_000001.10:g.237947518A>G , CM000663.1:g.237947518A>G GRCh37
NC_000001.9:g.236014141A>G NCBI36
NG_008799.2:g.746817A>G
NG_008799.3:g.747035A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000609119.2:c.*3598A>G ENSP00000499659.2:n.*3598A>G
ENST00000659194.3:c.12494A>G ENSP00000499653.3:p.Lys4165Arg
ENST00000660292.2:c.12527A>G ENSP00000499787.2:p.Lys4176Arg
ENST00000659194.2:c.4683A>G
ENST00000366574.7:c.12506A>G MANE Select ENSP00000355533.2:p.Lys4169Arg
ENST00000659194.1:c.4683A>G
ENST00000660292.1:c.2559A>G
ENST00000360064.7:c.12458A>G ENSP00000353174.7:p.Lys4153Arg
ENST00000366574.6:c.12506A>G ENSP00000355533.2:p.Lys4169Arg
ENST00000609119.1:n.3701A>G
NM_001035.2:c.12506A>G NP_001026.2:p.Lys4169Arg
XM_006711802.2:c.12560A>G XP_006711865.1:p.Lys4187Arg
XM_006711803.2:c.12557A>G XP_006711866.1:p.Lys4186Arg
XM_006711804.2:c.12536A>G XP_006711867.1:p.Lys4179Arg
XM_006711805.2:c.12530A>G XP_006711868.1:p.Lys4177Arg
XM_006711806.2:c.12524A>G XP_006711869.1:p.Lys4175Arg
XM_006711807.2:c.12500A>G XP_006711870.1:p.Lys4167Arg
XM_006711808.2:c.12323A>G XP_006711871.1:p.Lys4108Arg
XM_006711810.2:c.12467A>G XP_006711873.1:p.Lys4156Arg
XM_006711802.3:c.12560A>G XP_006711865.1:p.Lys4187Arg
XM_006711803.3:c.12557A>G XP_006711866.1:p.Lys4186Arg
XM_006711804.3:c.12536A>G XP_006711867.1:p.Lys4179Arg
XM_006711805.3:c.12530A>G XP_006711868.1:p.Lys4177Arg
XM_006711806.3:c.12524A>G XP_006711869.1:p.Lys4175Arg
XM_006711807.3:c.12500A>G XP_006711870.1:p.Lys4167Arg
XM_006711808.3:c.12323A>G XP_006711871.1:p.Lys4108Arg
XM_006711810.3:c.12467A>G XP_006711873.1:p.Lys4156Arg
XM_017002028.1:c.12539A>G XP_016857517.1:p.Lys4180Arg
NM_001035.3:c.12506A>G MANE Select NP_001026.2:p.Lys4169Arg