Canonical Allele Identifier: CA345413698

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947603C>G (hg19) ; chr1:g.237784303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784303C>G , CM000663.2:g.237784303C>G	GRCh38
NC_000001.10:g.237947603C>G , CM000663.1:g.237947603C>G	GRCh37
NC_000001.9:g.236014226C>G	NCBI36
NG_008799.2:g.746902C>G
NG_008799.3:g.747120C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3683C>G	ENSP00000499659.2:n.*3683C>G
ENST00000659194.3:c.12579C>G	ENSP00000499653.3:p.Ile4193Met
ENST00000660292.2:c.12612C>G	ENSP00000499787.2:p.Ile4204Met
ENST00000659194.2:c.4768C>G
ENST00000366574.7:c.12591C>G MANE Select	ENSP00000355533.2:p.Ile4197Met
ENST00000659194.1:c.4768C>G
ENST00000660292.1:c.2644C>G
ENST00000360064.7:c.12543C>G	ENSP00000353174.7:p.Ile4181Met
ENST00000366574.6:c.12591C>G	ENSP00000355533.2:p.Ile4197Met
ENST00000609119.1:n.3786C>G
NM_001035.2:c.12591C>G	NP_001026.2:p.Ile4197Met
XM_006711802.2:c.12645C>G	XP_006711865.1:p.Ile4215Met
XM_006711803.2:c.12642C>G	XP_006711866.1:p.Ile4214Met
XM_006711804.2:c.12621C>G	XP_006711867.1:p.Ile4207Met
XM_006711805.2:c.12615C>G	XP_006711868.1:p.Ile4205Met
XM_006711806.2:c.12609C>G	XP_006711869.1:p.Ile4203Met
XM_006711807.2:c.12585C>G	XP_006711870.1:p.Ile4195Met
XM_006711808.2:c.12408C>G	XP_006711871.1:p.Ile4136Met
XM_006711810.2:c.12552C>G	XP_006711873.1:p.Ile4184Met
XM_006711802.3:c.12645C>G	XP_006711865.1:p.Ile4215Met
XM_006711803.3:c.12642C>G	XP_006711866.1:p.Ile4214Met
XM_006711804.3:c.12621C>G	XP_006711867.1:p.Ile4207Met
XM_006711805.3:c.12615C>G	XP_006711868.1:p.Ile4205Met
XM_006711806.3:c.12609C>G	XP_006711869.1:p.Ile4203Met
XM_006711807.3:c.12585C>G	XP_006711870.1:p.Ile4195Met
XM_006711808.3:c.12408C>G	XP_006711871.1:p.Ile4136Met
XM_006711810.3:c.12552C>G	XP_006711873.1:p.Ile4184Met
XM_017002028.1:c.12624C>G	XP_016857517.1:p.Ile4208Met
NM_001035.3:c.12591C>G MANE Select	NP_001026.2:p.Ile4197Met