Canonical Allele Identifier: CA2487417995

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237627938_237627939delinsCG , CM000663.2:g.237627938_237627939delinsCG	GRCh38
NC_000001.10:g.237791238_237791239delinsCG , CM000663.1:g.237791238_237791239delinsCG	GRCh37
NC_000001.9:g.235857861_235857862delinsCG	NCBI36
NG_008799.2:g.590537_590538delinsCG
NG_008799.3:g.590755_590756delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.6298_6299delinsCG	ENSP00000499659.2:p.Arg2100=
ENST00000659194.3:c.6298_6299delinsCG	ENSP00000499653.3:p.Arg2100=
ENST00000660292.2:c.6298_6299delinsCG	ENSP00000499787.2:p.Arg2100=
ENST00000366574.7:c.6298_6299delinsCG MANE Select	ENSP00000355533.2:p.Arg2100=
ENST00000360064.7:c.6250_6251delinsCG	ENSP00000353174.7:p.Arg2084=
ENST00000366574.6:c.6298_6299delinsCG	ENSP00000355533.2:p.Arg2100=
NM_001035.2:c.6298_6299delinsCG	NP_001026.2:p.Arg2100=
XM_006711802.2:c.6328_6329delinsCG	XP_006711865.1:p.Arg2110=
XM_006711803.2:c.6325_6326delinsCG	XP_006711866.1:p.Arg2109=
XM_006711804.2:c.6328_6329delinsCG	XP_006711867.1:p.Arg2110=
XM_006711805.2:c.6298_6299delinsCG	XP_006711868.1:p.Arg2100=
XM_006711806.2:c.6328_6329delinsCG	XP_006711869.1:p.Arg2110=
XM_006711807.2:c.6328_6329delinsCG	XP_006711870.1:p.Arg2110=
XM_006711808.2:c.6328_6329delinsCG	XP_006711871.1:p.Arg2110=
XM_006711809.2:c.6328_6329delinsCG	XP_006711872.1:p.Arg2110=
XM_006711810.2:c.6295_6296delinsCG	XP_006711873.1:p.Arg2099=
XR_949152.1:n.6609_6610delinsCG
XM_006711802.3:c.6328_6329delinsCG	XP_006711865.1:p.Arg2110=
XM_006711803.3:c.6325_6326delinsCG	XP_006711866.1:p.Arg2109=
XM_006711804.3:c.6328_6329delinsCG	XP_006711867.1:p.Arg2110=
XM_006711805.3:c.6298_6299delinsCG	XP_006711868.1:p.Arg2100=
XM_006711806.3:c.6328_6329delinsCG	XP_006711869.1:p.Arg2110=
XM_006711807.3:c.6328_6329delinsCG	XP_006711870.1:p.Arg2110=
XM_006711808.3:c.6328_6329delinsCG	XP_006711871.1:p.Arg2110=
XM_006711810.3:c.6295_6296delinsCG	XP_006711873.1:p.Arg2099=
XM_017002028.1:c.6307_6308delinsCG	XP_016857517.1:p.Arg2103=
XR_002957299.1:n.6642_6643delinsCG
XR_949152.2:n.6642_6643delinsCG
NM_001035.3:c.6298_6299delinsCG MANE Select	NP_001026.2:p.Arg2100=