Canonical Allele Identifier: CA424032159

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947342C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784042C>G , CM000663.2:g.237784042C>G	GRCh38
NC_000001.10:g.237947342C>G , CM000663.1:g.237947342C>G	GRCh37
NC_000001.9:g.236013965C>G	NCBI36
NG_008799.2:g.746641C>G
NG_008799.3:g.746859C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3422C>G	ENSP00000499659.2:n.*3422C>G
ENST00000659194.3:c.12318C>G	ENSP00000499653.3:p.Pro4106=
ENST00000660292.2:c.12351C>G	ENSP00000499787.2:p.Pro4117=
ENST00000659194.2:c.4507C>G
ENST00000366574.7:c.12330C>G MANE Select	ENSP00000355533.2:p.Pro4110=
ENST00000659194.1:c.4507C>G
ENST00000660292.1:c.2383C>G
ENST00000360064.7:c.12282C>G	ENSP00000353174.7:p.Pro4094=
ENST00000366574.6:c.12330C>G	ENSP00000355533.2:p.Pro4110=
ENST00000609119.1:n.3525C>G
NM_001035.2:c.12330C>G	NP_001026.2:p.Pro4110=
XM_006711802.2:c.12384C>G	XP_006711865.1:p.Pro4128=
XM_006711803.2:c.12381C>G	XP_006711866.1:p.Pro4127=
XM_006711804.2:c.12360C>G	XP_006711867.1:p.Pro4120=
XM_006711805.2:c.12354C>G	XP_006711868.1:p.Pro4118=
XM_006711806.2:c.12348C>G	XP_006711869.1:p.Pro4116=
XM_006711807.2:c.12324C>G	XP_006711870.1:p.Pro4108=
XM_006711808.2:c.12147C>G	XP_006711871.1:p.Pro4049=
XM_006711810.2:c.12291C>G	XP_006711873.1:p.Pro4097=
XM_006711802.3:c.12384C>G	XP_006711865.1:p.Pro4128=
XM_006711803.3:c.12381C>G	XP_006711866.1:p.Pro4127=
XM_006711804.3:c.12360C>G	XP_006711867.1:p.Pro4120=
XM_006711805.3:c.12354C>G	XP_006711868.1:p.Pro4118=
XM_006711806.3:c.12348C>G	XP_006711869.1:p.Pro4116=
XM_006711807.3:c.12324C>G	XP_006711870.1:p.Pro4108=
XM_006711808.3:c.12147C>G	XP_006711871.1:p.Pro4049=
XM_006711810.3:c.12291C>G	XP_006711873.1:p.Pro4097=
XM_017002028.1:c.12363C>G	XP_016857517.1:p.Pro4121=
NM_001035.3:c.12330C>G MANE Select	NP_001026.2:p.Pro4110=