Canonical Allele Identifier: CA345413847

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947668A>T (hg19) ; chr1:g.237784368A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784368A>T , CM000663.2:g.237784368A>T	GRCh38
NC_000001.10:g.237947668A>T , CM000663.1:g.237947668A>T	GRCh37
NC_000001.9:g.236014291A>T	NCBI36
NG_008799.2:g.746967A>T
NG_008799.3:g.747185A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3748A>T	ENSP00000499659.2:n.*3748A>T
ENST00000659194.3:c.12644A>T	ENSP00000499653.3:p.Glu4215Val
ENST00000660292.2:c.12677A>T	ENSP00000499787.2:p.Glu4226Val
ENST00000659194.2:c.4833A>T
ENST00000366574.7:c.12656A>T MANE Select	ENSP00000355533.2:p.Glu4219Val
ENST00000659194.1:c.4833A>T
ENST00000660292.1:c.2709A>T
ENST00000360064.7:c.12608A>T	ENSP00000353174.7:p.Glu4203Val
ENST00000366574.6:c.12656A>T	ENSP00000355533.2:p.Glu4219Val
ENST00000609119.1:n.3851A>T
NM_001035.2:c.12656A>T	NP_001026.2:p.Glu4219Val
XM_006711802.2:c.12710A>T	XP_006711865.1:p.Glu4237Val
XM_006711803.2:c.12707A>T	XP_006711866.1:p.Glu4236Val
XM_006711804.2:c.12686A>T	XP_006711867.1:p.Glu4229Val
XM_006711805.2:c.12680A>T	XP_006711868.1:p.Glu4227Val
XM_006711806.2:c.12674A>T	XP_006711869.1:p.Glu4225Val
XM_006711807.2:c.12650A>T	XP_006711870.1:p.Glu4217Val
XM_006711808.2:c.12473A>T	XP_006711871.1:p.Glu4158Val
XM_006711810.2:c.12617A>T	XP_006711873.1:p.Glu4206Val
XM_006711802.3:c.12710A>T	XP_006711865.1:p.Glu4237Val
XM_006711803.3:c.12707A>T	XP_006711866.1:p.Glu4236Val
XM_006711804.3:c.12686A>T	XP_006711867.1:p.Glu4229Val
XM_006711805.3:c.12680A>T	XP_006711868.1:p.Glu4227Val
XM_006711806.3:c.12674A>T	XP_006711869.1:p.Glu4225Val
XM_006711807.3:c.12650A>T	XP_006711870.1:p.Glu4217Val
XM_006711808.3:c.12473A>T	XP_006711871.1:p.Glu4158Val
XM_006711810.3:c.12617A>T	XP_006711873.1:p.Glu4206Val
XM_017002028.1:c.12689A>T	XP_016857517.1:p.Glu4230Val
NM_001035.3:c.12656A>T MANE Select	NP_001026.2:p.Glu4219Val