Canonical Allele Identifier: CA006532

Gene: RYR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237709015C>A , CM000663.2:g.237709015C>A	GRCh38
NC_000001.10:g.237872315C>A , CM000663.1:g.237872315C>A	GRCh37
NC_000001.9:g.235938938C>A	NCBI36
NG_008799.2:g.671614C>A
NG_008799.3:g.671832C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*1094C>A	ENSP00000499659.2:n.*1094C>A
ENST00000659194.3:c.10059C>A	ENSP00000499653.3:p.Leu3353=
ENST00000660292.2:c.10059C>A	ENSP00000499787.2:p.Leu3353=
ENST00000659194.2:c.2248C>A
ENST00000366574.7:c.10059C>A MANE Select	ENSP00000355533.2:p.Leu3353=
ENST00000659194.1:c.2248C>A
ENST00000660292.1:c.91C>A
ENST00000360064.7:c.10011C>A	ENSP00000353174.7:p.Leu3337=
ENST00000366574.6:c.10059C>A	ENSP00000355533.2:p.Leu3353=
ENST00000609119.1:n.1197C>A
NM_001035.2:c.10059C>A	NP_001026.2:p.Leu3353=
XM_006711802.2:c.10089C>A	XP_006711865.1:p.Leu3363=
XM_006711803.2:c.10086C>A	XP_006711866.1:p.Leu3362=
XM_006711804.2:c.10089C>A	XP_006711867.1:p.Leu3363=
XM_006711805.2:c.10059C>A	XP_006711868.1:p.Leu3353=
XM_006711806.2:c.10089C>A	XP_006711869.1:p.Leu3363=
XM_006711807.2:c.10089C>A	XP_006711870.1:p.Leu3363=
XM_006711808.2:c.9852C>A	XP_006711871.1:p.Leu3284=
XM_006711810.2:c.10056C>A	XP_006711873.1:p.Leu3352=
XM_006711802.3:c.10089C>A	XP_006711865.1:p.Leu3363=
XM_006711803.3:c.10086C>A	XP_006711866.1:p.Leu3362=
XM_006711804.3:c.10089C>A	XP_006711867.1:p.Leu3363=
XM_006711805.3:c.10059C>A	XP_006711868.1:p.Leu3353=
XM_006711806.3:c.10089C>A	XP_006711869.1:p.Leu3363=
XM_006711807.3:c.10089C>A	XP_006711870.1:p.Leu3363=
XM_006711808.3:c.9852C>A	XP_006711871.1:p.Leu3284=
XM_006711810.3:c.10056C>A	XP_006711873.1:p.Leu3352=
XM_017002028.1:c.10068C>A	XP_016857517.1:p.Leu3356=
NM_001035.3:c.10059C>A MANE Select	NP_001026.2:p.Leu3353=