Canonical Allele Identifier: CA345413514

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947524A>T (hg19) ; chr1:g.237784224A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784224A>T , CM000663.2:g.237784224A>T	GRCh38
NC_000001.10:g.237947524A>T , CM000663.1:g.237947524A>T	GRCh37
NC_000001.9:g.236014147A>T	NCBI36
NG_008799.2:g.746823A>T
NG_008799.3:g.747041A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000609119.2:c.*3604A>T	ENSP00000499659.2:n.*3604A>T
ENST00000659194.3:c.12500A>T	ENSP00000499653.3:p.Gln4167Leu
ENST00000660292.2:c.12533A>T	ENSP00000499787.2:p.Gln4178Leu
ENST00000659194.2:c.4689A>T
ENST00000366574.7:c.12512A>T MANE Select	ENSP00000355533.2:p.Gln4171Leu
ENST00000659194.1:c.4689A>T
ENST00000660292.1:c.2565A>T
ENST00000360064.7:c.12464A>T	ENSP00000353174.7:p.Gln4155Leu
ENST00000366574.6:c.12512A>T	ENSP00000355533.2:p.Gln4171Leu
ENST00000609119.1:n.3707A>T
NM_001035.2:c.12512A>T	NP_001026.2:p.Gln4171Leu
XM_006711802.2:c.12566A>T	XP_006711865.1:p.Gln4189Leu
XM_006711803.2:c.12563A>T	XP_006711866.1:p.Gln4188Leu
XM_006711804.2:c.12542A>T	XP_006711867.1:p.Gln4181Leu
XM_006711805.2:c.12536A>T	XP_006711868.1:p.Gln4179Leu
XM_006711806.2:c.12530A>T	XP_006711869.1:p.Gln4177Leu
XM_006711807.2:c.12506A>T	XP_006711870.1:p.Gln4169Leu
XM_006711808.2:c.12329A>T	XP_006711871.1:p.Gln4110Leu
XM_006711810.2:c.12473A>T	XP_006711873.1:p.Gln4158Leu
XM_006711802.3:c.12566A>T	XP_006711865.1:p.Gln4189Leu
XM_006711803.3:c.12563A>T	XP_006711866.1:p.Gln4188Leu
XM_006711804.3:c.12542A>T	XP_006711867.1:p.Gln4181Leu
XM_006711805.3:c.12536A>T	XP_006711868.1:p.Gln4179Leu
XM_006711806.3:c.12530A>T	XP_006711869.1:p.Gln4177Leu
XM_006711807.3:c.12506A>T	XP_006711870.1:p.Gln4169Leu
XM_006711808.3:c.12329A>T	XP_006711871.1:p.Gln4110Leu
XM_006711810.3:c.12473A>T	XP_006711873.1:p.Gln4158Leu
XM_017002028.1:c.12545A>T	XP_016857517.1:p.Gln4182Leu
NM_001035.3:c.12512A>T MANE Select	NP_001026.2:p.Gln4171Leu