Canonical Allele Identifier: CA345413096

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947395A>G (hg19) ; chr1:g.237784095A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784095A>G , CM000663.2:g.237784095A>G	GRCh38
NC_000001.10:g.237947395A>G , CM000663.1:g.237947395A>G	GRCh37
NC_000001.9:g.236014018A>G	NCBI36
NG_008799.2:g.746694A>G
NG_008799.3:g.746912A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3475A>G	ENSP00000499659.2:n.*3475A>G
ENST00000659194.3:c.12371A>G	ENSP00000499653.3:p.Tyr4124Cys
ENST00000660292.2:c.12404A>G	ENSP00000499787.2:p.Tyr4135Cys
ENST00000659194.2:c.4560A>G
ENST00000366574.7:c.12383A>G MANE Select	ENSP00000355533.2:p.Tyr4128Cys
ENST00000659194.1:c.4560A>G
ENST00000660292.1:c.2436A>G
ENST00000360064.7:c.12335A>G	ENSP00000353174.7:p.Tyr4112Cys
ENST00000366574.6:c.12383A>G	ENSP00000355533.2:p.Tyr4128Cys
ENST00000609119.1:n.3578A>G
NM_001035.2:c.12383A>G	NP_001026.2:p.Tyr4128Cys
XM_006711802.2:c.12437A>G	XP_006711865.1:p.Tyr4146Cys
XM_006711803.2:c.12434A>G	XP_006711866.1:p.Tyr4145Cys
XM_006711804.2:c.12413A>G	XP_006711867.1:p.Tyr4138Cys
XM_006711805.2:c.12407A>G	XP_006711868.1:p.Tyr4136Cys
XM_006711806.2:c.12401A>G	XP_006711869.1:p.Tyr4134Cys
XM_006711807.2:c.12377A>G	XP_006711870.1:p.Tyr4126Cys
XM_006711808.2:c.12200A>G	XP_006711871.1:p.Tyr4067Cys
XM_006711810.2:c.12344A>G	XP_006711873.1:p.Tyr4115Cys
XM_006711802.3:c.12437A>G	XP_006711865.1:p.Tyr4146Cys
XM_006711803.3:c.12434A>G	XP_006711866.1:p.Tyr4145Cys
XM_006711804.3:c.12413A>G	XP_006711867.1:p.Tyr4138Cys
XM_006711805.3:c.12407A>G	XP_006711868.1:p.Tyr4136Cys
XM_006711806.3:c.12401A>G	XP_006711869.1:p.Tyr4134Cys
XM_006711807.3:c.12377A>G	XP_006711870.1:p.Tyr4126Cys
XM_006711808.3:c.12200A>G	XP_006711871.1:p.Tyr4067Cys
XM_006711810.3:c.12344A>G	XP_006711873.1:p.Tyr4115Cys
XM_017002028.1:c.12416A>G	XP_016857517.1:p.Tyr4139Cys
NM_001035.3:c.12383A>G MANE Select	NP_001026.2:p.Tyr4128Cys