Canonical Allele Identifier: CA424051751

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237972320T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237809020T>C , CM000663.2:g.237809020T>C	GRCh38
NC_000001.10:g.237972320T>C , CM000663.1:g.237972320T>C	GRCh37
NC_000001.9:g.236038943T>C	NCBI36
NG_008799.2:g.771619T>C
NG_008799.3:g.771837T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5510T>C	ENSP00000499659.2:n.*5510T>C
ENST00000659194.3:c.14400T>C	ENSP00000499653.3:p.Cys4800=
ENST00000660292.2:c.14439T>C	ENSP00000499787.2:p.Cys4813=
ENST00000659194.2:c.6589T>C
ENST00000366574.7:c.14418T>C MANE Select	ENSP00000355533.2:p.Cys4806=
ENST00000360064.7:c.14367T>C	ENSP00000353174.7:p.Cys4789=
ENST00000366574.6:c.14418T>C	ENSP00000355533.2:p.Cys4806=
ENST00000608590.5:n.929T>C
NM_001035.2:c.14418T>C	NP_001026.2:p.Cys4806=
XM_006711802.2:c.14472T>C	XP_006711865.1:p.Cys4824=
XM_006711803.2:c.14469T>C	XP_006711866.1:p.Cys4823=
XM_006711804.2:c.14448T>C	XP_006711867.1:p.Cys4816=
XM_006711805.2:c.14442T>C	XP_006711868.1:p.Cys4814=
XM_006711806.2:c.14436T>C	XP_006711869.1:p.Cys4812=
XM_006711807.2:c.14412T>C	XP_006711870.1:p.Cys4804=
XM_006711808.2:c.14235T>C	XP_006711871.1:p.Cys4745=
XM_006711810.2:c.14379T>C	XP_006711873.1:p.Cys4793=
XM_006711802.3:c.14472T>C	XP_006711865.1:p.Cys4824=
XM_006711803.3:c.14469T>C	XP_006711866.1:p.Cys4823=
XM_006711804.3:c.14448T>C	XP_006711867.1:p.Cys4816=
XM_006711805.3:c.14442T>C	XP_006711868.1:p.Cys4814=
XM_006711806.3:c.14436T>C	XP_006711869.1:p.Cys4812=
XM_006711807.3:c.14412T>C	XP_006711870.1:p.Cys4804=
XM_006711808.3:c.14235T>C	XP_006711871.1:p.Cys4745=
XM_006711810.3:c.14379T>C	XP_006711873.1:p.Cys4793=
XM_017002028.1:c.14451T>C	XP_016857517.1:p.Cys4817=
NM_001035.3:c.14418T>C MANE Select	NP_001026.2:p.Cys4806=