Canonical Allele Identifier: CA345409242

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237942013G>A (hg19) ; chr1:g.237778713G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237778713G>A , CM000663.2:g.237778713G>A	GRCh38
NC_000001.10:g.237942013G>A , CM000663.1:g.237942013G>A	GRCh37
NC_000001.9:g.236008636G>A	NCBI36
NG_008799.2:g.741312G>A
NG_008799.3:g.741530G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*2915G>A	ENSP00000499659.2:n.*2915G>A
ENST00000659194.3:c.11811G>A	ENSP00000499653.3:p.Trp3937Ter
ENST00000660292.2:c.11844G>A	ENSP00000499787.2:p.Trp3948Ter
ENST00000659194.2:c.4000G>A
ENST00000366574.7:c.11823G>A MANE Select	ENSP00000355533.2:p.Trp3941Ter
ENST00000659194.1:c.4000G>A
ENST00000660292.1:c.1876G>A
ENST00000360064.7:c.11775G>A	ENSP00000353174.7:p.Trp3925Ter
ENST00000366574.6:c.11823G>A	ENSP00000355533.2:p.Trp3941Ter
ENST00000609119.1:n.3018G>A
NM_001035.2:c.11823G>A	NP_001026.2:p.Trp3941Ter
XM_006711802.2:c.11877G>A	XP_006711865.1:p.Trp3959Ter
XM_006711803.2:c.11874G>A	XP_006711866.1:p.Trp3958Ter
XM_006711804.2:c.11853G>A	XP_006711867.1:p.Trp3951Ter
XM_006711805.2:c.11847G>A	XP_006711868.1:p.Trp3949Ter
XM_006711806.2:c.11841G>A	XP_006711869.1:p.Trp3947Ter
XM_006711807.2:c.11817G>A	XP_006711870.1:p.Trp3939Ter
XM_006711808.2:c.11640G>A	XP_006711871.1:p.Trp3880Ter
XM_006711810.2:c.11784G>A	XP_006711873.1:p.Trp3928Ter
XM_006711802.3:c.11877G>A	XP_006711865.1:p.Trp3959Ter
XM_006711803.3:c.11874G>A	XP_006711866.1:p.Trp3958Ter
XM_006711804.3:c.11853G>A	XP_006711867.1:p.Trp3951Ter
XM_006711805.3:c.11847G>A	XP_006711868.1:p.Trp3949Ter
XM_006711806.3:c.11841G>A	XP_006711869.1:p.Trp3947Ter
XM_006711807.3:c.11817G>A	XP_006711870.1:p.Trp3939Ter
XM_006711808.3:c.11640G>A	XP_006711871.1:p.Trp3880Ter
XM_006711810.3:c.11784G>A	XP_006711873.1:p.Trp3928Ter
XM_017002028.1:c.11856G>A	XP_016857517.1:p.Trp3952Ter
NM_001035.3:c.11823G>A MANE Select	NP_001026.2:p.Trp3941Ter