Canonical Allele Identifier: CA345413420

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947488A>G (hg19) ; chr1:g.237784188A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784188A>G , CM000663.2:g.237784188A>G	GRCh38
NC_000001.10:g.237947488A>G , CM000663.1:g.237947488A>G	GRCh37
NC_000001.9:g.236014111A>G	NCBI36
NG_008799.2:g.746787A>G
NG_008799.3:g.747005A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3568A>G	ENSP00000499659.2:n.*3568A>G
ENST00000659194.3:c.12464A>G	ENSP00000499653.3:p.Gln4155Arg
ENST00000660292.2:c.12497A>G	ENSP00000499787.2:p.Gln4166Arg
ENST00000659194.2:c.4653A>G
ENST00000366574.7:c.12476A>G MANE Select	ENSP00000355533.2:p.Gln4159Arg
ENST00000659194.1:c.4653A>G
ENST00000660292.1:c.2529A>G
ENST00000360064.7:c.12428A>G	ENSP00000353174.7:p.Gln4143Arg
ENST00000366574.6:c.12476A>G	ENSP00000355533.2:p.Gln4159Arg
ENST00000609119.1:n.3671A>G
NM_001035.2:c.12476A>G	NP_001026.2:p.Gln4159Arg
XM_006711802.2:c.12530A>G	XP_006711865.1:p.Gln4177Arg
XM_006711803.2:c.12527A>G	XP_006711866.1:p.Gln4176Arg
XM_006711804.2:c.12506A>G	XP_006711867.1:p.Gln4169Arg
XM_006711805.2:c.12500A>G	XP_006711868.1:p.Gln4167Arg
XM_006711806.2:c.12494A>G	XP_006711869.1:p.Gln4165Arg
XM_006711807.2:c.12470A>G	XP_006711870.1:p.Gln4157Arg
XM_006711808.2:c.12293A>G	XP_006711871.1:p.Gln4098Arg
XM_006711810.2:c.12437A>G	XP_006711873.1:p.Gln4146Arg
XM_006711802.3:c.12530A>G	XP_006711865.1:p.Gln4177Arg
XM_006711803.3:c.12527A>G	XP_006711866.1:p.Gln4176Arg
XM_006711804.3:c.12506A>G	XP_006711867.1:p.Gln4169Arg
XM_006711805.3:c.12500A>G	XP_006711868.1:p.Gln4167Arg
XM_006711806.3:c.12494A>G	XP_006711869.1:p.Gln4165Arg
XM_006711807.3:c.12470A>G	XP_006711870.1:p.Gln4157Arg
XM_006711808.3:c.12293A>G	XP_006711871.1:p.Gln4098Arg
XM_006711810.3:c.12437A>G	XP_006711873.1:p.Gln4146Arg
XM_017002028.1:c.12509A>G	XP_016857517.1:p.Gln4170Arg
NM_001035.3:c.12476A>G MANE Select	NP_001026.2:p.Gln4159Arg