Canonical Allele Identifier: CA345413462

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947503A>G (hg19) ; chr1:g.237784203A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784203A>G , CM000663.2:g.237784203A>G	GRCh38
NC_000001.10:g.237947503A>G , CM000663.1:g.237947503A>G	GRCh37
NC_000001.9:g.236014126A>G	NCBI36
NG_008799.2:g.746802A>G
NG_008799.3:g.747020A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3583A>G	ENSP00000499659.2:n.*3583A>G
ENST00000659194.3:c.12479A>G	ENSP00000499653.3:p.Gln4160Arg
ENST00000660292.2:c.12512A>G	ENSP00000499787.2:p.Gln4171Arg
ENST00000659194.2:c.4668A>G
ENST00000366574.7:c.12491A>G MANE Select	ENSP00000355533.2:p.Gln4164Arg
ENST00000659194.1:c.4668A>G
ENST00000660292.1:c.2544A>G
ENST00000360064.7:c.12443A>G	ENSP00000353174.7:p.Gln4148Arg
ENST00000366574.6:c.12491A>G	ENSP00000355533.2:p.Gln4164Arg
ENST00000609119.1:n.3686A>G
NM_001035.2:c.12491A>G	NP_001026.2:p.Gln4164Arg
XM_006711802.2:c.12545A>G	XP_006711865.1:p.Gln4182Arg
XM_006711803.2:c.12542A>G	XP_006711866.1:p.Gln4181Arg
XM_006711804.2:c.12521A>G	XP_006711867.1:p.Gln4174Arg
XM_006711805.2:c.12515A>G	XP_006711868.1:p.Gln4172Arg
XM_006711806.2:c.12509A>G	XP_006711869.1:p.Gln4170Arg
XM_006711807.2:c.12485A>G	XP_006711870.1:p.Gln4162Arg
XM_006711808.2:c.12308A>G	XP_006711871.1:p.Gln4103Arg
XM_006711810.2:c.12452A>G	XP_006711873.1:p.Gln4151Arg
XM_006711802.3:c.12545A>G	XP_006711865.1:p.Gln4182Arg
XM_006711803.3:c.12542A>G	XP_006711866.1:p.Gln4181Arg
XM_006711804.3:c.12521A>G	XP_006711867.1:p.Gln4174Arg
XM_006711805.3:c.12515A>G	XP_006711868.1:p.Gln4172Arg
XM_006711806.3:c.12509A>G	XP_006711869.1:p.Gln4170Arg
XM_006711807.3:c.12485A>G	XP_006711870.1:p.Gln4162Arg
XM_006711808.3:c.12308A>G	XP_006711871.1:p.Gln4103Arg
XM_006711810.3:c.12452A>G	XP_006711873.1:p.Gln4151Arg
XM_017002028.1:c.12524A>G	XP_016857517.1:p.Gln4175Arg
NM_001035.3:c.12491A>G MANE Select	NP_001026.2:p.Gln4164Arg