Canonical Allele Identifier: CA2748275636

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237566481_237566482insCCCCC , CM000663.2:g.237566481_237566482insCCCCC	GRCh38
NC_000001.10:g.237729781_237729782insCCCCC , CM000663.1:g.237729781_237729782insCCCCC	GRCh37
NC_000001.9:g.235796404_235796405insCCCCC	NCBI36
NG_008799.2:g.529080_529081insCCCCC
NG_008799.3:g.529298_529299insCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.3215-86_3215-85insCCCCC	ENSP00000499659.2:n.3215-86_3215-85insCCCCC
ENST00000659194.3:c.3215-86_3215-85insCCCCC	ENSP00000499653.3:n.3215-86_3215-85insCCCCC
ENST00000660292.2:c.3215-86_3215-85insCCCCC	ENSP00000499787.2:n.3215-86_3215-85insCCCCC
ENST00000366574.7:c.3215-86_3215-85insCCCCC MANE Select	ENSP00000355533.2:n.3215-86_3215-85insCCCCC
ENST00000360064.7:c.3167-86_3167-85insCCCCC	ENSP00000353174.7:n.3167-86_3167-85insCCCCC
ENST00000366574.6:c.3215-86_3215-85insCCCCC	ENSP00000355533.2:n.3215-86_3215-85insCCCCC
NM_001035.2:c.3215-86_3215-85insCCCCC	NP_001026.2:n.3215-86_3215-85insCCCCC
XM_006711802.2:c.3215-86_3215-85insCCCCC	XP_006711865.1:n.3215-86_3215-85insCCCCC
XM_006711803.2:c.3215-89_3215-88insCCCCC	XP_006711866.1:n.3215-89_3215-88insCCCCC
XM_006711804.2:c.3215-86_3215-85insCCCCC	XP_006711867.1:n.3215-86_3215-85insCCCCC
XM_006711805.2:c.3215-86_3215-85insCCCCC	XP_006711868.1:n.3215-86_3215-85insCCCCC
XM_006711806.2:c.3215-86_3215-85insCCCCC	XP_006711869.1:n.3215-86_3215-85insCCCCC
XM_006711807.2:c.3215-86_3215-85insCCCCC	XP_006711870.1:n.3215-86_3215-85insCCCCC
XM_006711808.2:c.3215-86_3215-85insCCCCC	XP_006711871.1:n.3215-86_3215-85insCCCCC
XM_006711809.2:c.3215-86_3215-85insCCCCC	XP_006711872.1:n.3215-86_3215-85insCCCCC
XM_006711810.2:c.3215-89_3215-88insCCCCC	XP_006711873.1:n.3215-89_3215-88insCCCCC
XR_949152.1:n.3496-86_3496-85insCCCCC
XM_006711802.3:c.3215-86_3215-85insCCCCC	XP_006711865.1:n.3215-86_3215-85insCCCCC
XM_006711803.3:c.3215-89_3215-88insCCCCC	XP_006711866.1:n.3215-89_3215-88insCCCCC
XM_006711804.3:c.3215-86_3215-85insCCCCC	XP_006711867.1:n.3215-86_3215-85insCCCCC
XM_006711805.3:c.3215-86_3215-85insCCCCC	XP_006711868.1:n.3215-86_3215-85insCCCCC
XM_006711806.3:c.3215-86_3215-85insCCCCC	XP_006711869.1:n.3215-86_3215-85insCCCCC
XM_006711807.3:c.3215-86_3215-85insCCCCC	XP_006711870.1:n.3215-86_3215-85insCCCCC
XM_006711808.3:c.3215-86_3215-85insCCCCC	XP_006711871.1:n.3215-86_3215-85insCCCCC
XM_006711810.3:c.3215-89_3215-88insCCCCC	XP_006711873.1:n.3215-89_3215-88insCCCCC
XM_017002028.1:c.3194-86_3194-85insCCCCC	XP_016857517.1:n.3194-86_3194-85insCCCCC
XR_002957299.1:n.3529-86_3529-85insCCCCC
XR_949152.2:n.3529-86_3529-85insCCCCC
NM_001035.3:c.3215-86_3215-85insCCCCC MANE Select	NP_001026.2:n.3215-86_3215-85insCCCCC