Canonical Allele Identifier: CA2487327650

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237416750_237416757delinsACACACAC , CM000663.2:g.237416750_237416757delinsACACACAC	GRCh38
NC_000001.10:g.237580050_237580057delinsACACACAC , CM000663.1:g.237580050_237580057delinsACACACAC	GRCh37
NC_000001.9:g.235646673_235646680delinsACACACAC	NCBI36
NG_008799.2:g.379349_379356delinsACACACAC
NG_008799.3:g.379567_379574delinsACACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.774-299_774-292delinsACACACAC	ENSP00000499659.2:n.774-299_774-292delinsACACACAC
ENST00000659194.3:c.774-299_774-292delinsACACACAC	ENSP00000499653.3:n.774-299_774-292delinsACACACAC
ENST00000660292.2:c.774-299_774-292delinsACACACAC	ENSP00000499787.2:n.774-299_774-292delinsACACACAC
ENST00000366574.7:c.774-299_774-292delinsACACACAC MANE Select	ENSP00000355533.2:n.774-299_774-292delinsACACACAC
ENST00000360064.7:c.726-299_726-292delinsACACACAC	ENSP00000353174.7:n.726-299_726-292delinsACACACAC
ENST00000366574.6:c.774-299_774-292delinsACACACAC	ENSP00000355533.2:n.774-299_774-292delinsACACACAC
NM_001035.2:c.774-299_774-292delinsACACACAC	NP_001026.2:n.774-299_774-292delinsACACACAC
XM_006711802.2:c.774-299_774-292delinsACACACAC	XP_006711865.1:n.774-299_774-292delinsACACACAC
XM_006711803.2:c.774-299_774-292delinsACACACAC	XP_006711866.1:n.774-299_774-292delinsACACACAC
XM_006711804.2:c.774-299_774-292delinsACACACAC	XP_006711867.1:n.774-299_774-292delinsACACACAC
XM_006711805.2:c.774-299_774-292delinsACACACAC	XP_006711868.1:n.774-299_774-292delinsACACACAC
XM_006711806.2:c.774-299_774-292delinsACACACAC	XP_006711869.1:n.774-299_774-292delinsACACACAC
XM_006711807.2:c.774-299_774-292delinsACACACAC	XP_006711870.1:n.774-299_774-292delinsACACACAC
XM_006711808.2:c.774-299_774-292delinsACACACAC	XP_006711871.1:n.774-299_774-292delinsACACACAC
XM_006711809.2:c.774-299_774-292delinsACACACAC	XP_006711872.1:n.774-299_774-292delinsACACACAC
XM_006711810.2:c.774-299_774-292delinsACACACAC	XP_006711873.1:n.774-299_774-292delinsACACACAC
XR_949152.1:n.1055-299_1055-292delinsACACACAC
XM_006711802.3:c.774-299_774-292delinsACACACAC	XP_006711865.1:n.774-299_774-292delinsACACACAC
XM_006711803.3:c.774-299_774-292delinsACACACAC	XP_006711866.1:n.774-299_774-292delinsACACACAC
XM_006711804.3:c.774-299_774-292delinsACACACAC	XP_006711867.1:n.774-299_774-292delinsACACACAC
XM_006711805.3:c.774-299_774-292delinsACACACAC	XP_006711868.1:n.774-299_774-292delinsACACACAC
XM_006711806.3:c.774-299_774-292delinsACACACAC	XP_006711869.1:n.774-299_774-292delinsACACACAC
XM_006711807.3:c.774-299_774-292delinsACACACAC	XP_006711870.1:n.774-299_774-292delinsACACACAC
XM_006711808.3:c.774-299_774-292delinsACACACAC	XP_006711871.1:n.774-299_774-292delinsACACACAC
XM_006711810.3:c.774-299_774-292delinsACACACAC	XP_006711873.1:n.774-299_774-292delinsACACACAC
XM_017002028.1:c.753-299_753-292delinsACACACAC	XP_016857517.1:n.753-299_753-292delinsACACACAC
XR_002957299.1:n.1088-299_1088-292delinsACACACAC
XR_949152.2:n.1088-299_1088-292delinsACACACAC
NM_001035.3:c.774-299_774-292delinsACACACAC MANE Select	NP_001026.2:n.774-299_774-292delinsACACACAC