Canonical Allele Identifier: CA345413355

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947473A>T (hg19) ; chr1:g.237784173A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784173A>T , CM000663.2:g.237784173A>T	GRCh38
NC_000001.10:g.237947473A>T , CM000663.1:g.237947473A>T	GRCh37
NC_000001.9:g.236014096A>T	NCBI36
NG_008799.2:g.746772A>T
NG_008799.3:g.746990A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3553A>T	ENSP00000499659.2:n.*3553A>T
ENST00000659194.3:c.12449A>T	ENSP00000499653.3:p.Glu4150Val
ENST00000660292.2:c.12482A>T	ENSP00000499787.2:p.Glu4161Val
ENST00000659194.2:c.4638A>T
ENST00000366574.7:c.12461A>T MANE Select	ENSP00000355533.2:p.Glu4154Val
ENST00000659194.1:c.4638A>T
ENST00000660292.1:c.2514A>T
ENST00000360064.7:c.12413A>T	ENSP00000353174.7:p.Glu4138Val
ENST00000366574.6:c.12461A>T	ENSP00000355533.2:p.Glu4154Val
ENST00000609119.1:n.3656A>T
NM_001035.2:c.12461A>T	NP_001026.2:p.Glu4154Val
XM_006711802.2:c.12515A>T	XP_006711865.1:p.Glu4172Val
XM_006711803.2:c.12512A>T	XP_006711866.1:p.Glu4171Val
XM_006711804.2:c.12491A>T	XP_006711867.1:p.Glu4164Val
XM_006711805.2:c.12485A>T	XP_006711868.1:p.Glu4162Val
XM_006711806.2:c.12479A>T	XP_006711869.1:p.Glu4160Val
XM_006711807.2:c.12455A>T	XP_006711870.1:p.Glu4152Val
XM_006711808.2:c.12278A>T	XP_006711871.1:p.Glu4093Val
XM_006711810.2:c.12422A>T	XP_006711873.1:p.Glu4141Val
XM_006711802.3:c.12515A>T	XP_006711865.1:p.Glu4172Val
XM_006711803.3:c.12512A>T	XP_006711866.1:p.Glu4171Val
XM_006711804.3:c.12491A>T	XP_006711867.1:p.Glu4164Val
XM_006711805.3:c.12485A>T	XP_006711868.1:p.Glu4162Val
XM_006711806.3:c.12479A>T	XP_006711869.1:p.Glu4160Val
XM_006711807.3:c.12455A>T	XP_006711870.1:p.Glu4152Val
XM_006711808.3:c.12278A>T	XP_006711871.1:p.Glu4093Val
XM_006711810.3:c.12422A>T	XP_006711873.1:p.Glu4141Val
XM_017002028.1:c.12494A>T	XP_016857517.1:p.Glu4165Val
NM_001035.3:c.12461A>T MANE Select	NP_001026.2:p.Glu4154Val