Canonical Allele Identifier: CA345413445
Gene: RYR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237784197A>G , CM000663.2:g.237784197A>G GRCh38
NC_000001.10:g.237947497A>G , CM000663.1:g.237947497A>G GRCh37
NC_000001.9:g.236014120A>G NCBI36
NG_008799.2:g.746796A>G
NG_008799.3:g.747014A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.*3577A>G ENSP00000499659.2:n.*3577A>G
ENST00000659194.3:c.12473A>G ENSP00000499653.3:p.Lys4158Arg
ENST00000660292.2:c.12506A>G ENSP00000499787.2:p.Lys4169Arg
ENST00000659194.2:c.4662A>G
ENST00000366574.7:c.12485A>G MANE Select ENSP00000355533.2:p.Lys4162Arg
ENST00000659194.1:c.4662A>G
ENST00000660292.1:c.2538A>G
ENST00000360064.7:c.12437A>G ENSP00000353174.7:p.Lys4146Arg
ENST00000366574.6:c.12485A>G ENSP00000355533.2:p.Lys4162Arg
ENST00000609119.1:n.3680A>G
NM_001035.2:c.12485A>G NP_001026.2:p.Lys4162Arg
XM_006711802.2:c.12539A>G XP_006711865.1:p.Lys4180Arg
XM_006711803.2:c.12536A>G XP_006711866.1:p.Lys4179Arg
XM_006711804.2:c.12515A>G XP_006711867.1:p.Lys4172Arg
XM_006711805.2:c.12509A>G XP_006711868.1:p.Lys4170Arg
XM_006711806.2:c.12503A>G XP_006711869.1:p.Lys4168Arg
XM_006711807.2:c.12479A>G XP_006711870.1:p.Lys4160Arg
XM_006711808.2:c.12302A>G XP_006711871.1:p.Lys4101Arg
XM_006711810.2:c.12446A>G XP_006711873.1:p.Lys4149Arg
XM_006711802.3:c.12539A>G XP_006711865.1:p.Lys4180Arg
XM_006711803.3:c.12536A>G XP_006711866.1:p.Lys4179Arg
XM_006711804.3:c.12515A>G XP_006711867.1:p.Lys4172Arg
XM_006711805.3:c.12509A>G XP_006711868.1:p.Lys4170Arg
XM_006711806.3:c.12503A>G XP_006711869.1:p.Lys4168Arg
XM_006711807.3:c.12479A>G XP_006711870.1:p.Lys4160Arg
XM_006711808.3:c.12302A>G XP_006711871.1:p.Lys4101Arg
XM_006711810.3:c.12446A>G XP_006711873.1:p.Lys4149Arg
XM_017002028.1:c.12518A>G XP_016857517.1:p.Lys4173Arg
NM_001035.3:c.12485A>G MANE Select NP_001026.2:p.Lys4162Arg