Canonical Allele Identifier: CA345424401

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237972292A>T (hg19) ; chr1:g.237808992A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237808992A>T , CM000663.2:g.237808992A>T	GRCh38
NC_000001.10:g.237972292A>T , CM000663.1:g.237972292A>T	GRCh37
NC_000001.9:g.236038915A>T	NCBI36
NG_008799.2:g.771591A>T
NG_008799.3:g.771809A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5482A>T	ENSP00000499659.2:n.*5482A>T
ENST00000659194.3:c.14372A>T	ENSP00000499653.3:p.Glu4791Val
ENST00000660292.2:c.14411A>T	ENSP00000499787.2:p.Glu4804Val
ENST00000659194.2:c.6561A>T
ENST00000366574.7:c.14390A>T MANE Select	ENSP00000355533.2:p.Glu4797Val
ENST00000360064.7:c.14339A>T	ENSP00000353174.7:p.Glu4780Val
ENST00000366574.6:c.14390A>T	ENSP00000355533.2:p.Glu4797Val
ENST00000608590.5:n.901A>T
NM_001035.2:c.14390A>T	NP_001026.2:p.Glu4797Val
XM_006711802.2:c.14444A>T	XP_006711865.1:p.Glu4815Val
XM_006711803.2:c.14441A>T	XP_006711866.1:p.Glu4814Val
XM_006711804.2:c.14420A>T	XP_006711867.1:p.Glu4807Val
XM_006711805.2:c.14414A>T	XP_006711868.1:p.Glu4805Val
XM_006711806.2:c.14408A>T	XP_006711869.1:p.Glu4803Val
XM_006711807.2:c.14384A>T	XP_006711870.1:p.Glu4795Val
XM_006711808.2:c.14207A>T	XP_006711871.1:p.Glu4736Val
XM_006711810.2:c.14351A>T	XP_006711873.1:p.Glu4784Val
XM_006711802.3:c.14444A>T	XP_006711865.1:p.Glu4815Val
XM_006711803.3:c.14441A>T	XP_006711866.1:p.Glu4814Val
XM_006711804.3:c.14420A>T	XP_006711867.1:p.Glu4807Val
XM_006711805.3:c.14414A>T	XP_006711868.1:p.Glu4805Val
XM_006711806.3:c.14408A>T	XP_006711869.1:p.Glu4803Val
XM_006711807.3:c.14384A>T	XP_006711870.1:p.Glu4795Val
XM_006711808.3:c.14207A>T	XP_006711871.1:p.Glu4736Val
XM_006711810.3:c.14351A>T	XP_006711873.1:p.Glu4784Val
XM_017002028.1:c.14423A>T	XP_016857517.1:p.Glu4808Val
NM_001035.3:c.14390A>T MANE Select	NP_001026.2:p.Glu4797Val