Canonical Allele Identifier: CA2487327719

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237416853_237416855delinsCTT , CM000663.2:g.237416853_237416855delinsCTT	GRCh38
NC_000001.10:g.237580153_237580155delinsCTT , CM000663.1:g.237580153_237580155delinsCTT	GRCh37
NC_000001.9:g.235646776_235646778delinsCTT	NCBI36
NG_008799.2:g.379452_379454delinsCTT
NG_008799.3:g.379670_379672delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.774-196_774-194delinsCTT	ENSP00000499659.2:n.774-196_774-194delinsCTT
ENST00000659194.3:c.774-196_774-194delinsCTT	ENSP00000499653.3:n.774-196_774-194delinsCTT
ENST00000660292.2:c.774-196_774-194delinsCTT	ENSP00000499787.2:n.774-196_774-194delinsCTT
ENST00000366574.7:c.774-196_774-194delinsCTT MANE Select	ENSP00000355533.2:n.774-196_774-194delinsCTT
ENST00000360064.7:c.726-196_726-194delinsCTT	ENSP00000353174.7:n.726-196_726-194delinsCTT
ENST00000366574.6:c.774-196_774-194delinsCTT	ENSP00000355533.2:n.774-196_774-194delinsCTT
NM_001035.2:c.774-196_774-194delinsCTT	NP_001026.2:n.774-196_774-194delinsCTT
XM_006711802.2:c.774-196_774-194delinsCTT	XP_006711865.1:n.774-196_774-194delinsCTT
XM_006711803.2:c.774-196_774-194delinsCTT	XP_006711866.1:n.774-196_774-194delinsCTT
XM_006711804.2:c.774-196_774-194delinsCTT	XP_006711867.1:n.774-196_774-194delinsCTT
XM_006711805.2:c.774-196_774-194delinsCTT	XP_006711868.1:n.774-196_774-194delinsCTT
XM_006711806.2:c.774-196_774-194delinsCTT	XP_006711869.1:n.774-196_774-194delinsCTT
XM_006711807.2:c.774-196_774-194delinsCTT	XP_006711870.1:n.774-196_774-194delinsCTT
XM_006711808.2:c.774-196_774-194delinsCTT	XP_006711871.1:n.774-196_774-194delinsCTT
XM_006711809.2:c.774-196_774-194delinsCTT	XP_006711872.1:n.774-196_774-194delinsCTT
XM_006711810.2:c.774-196_774-194delinsCTT	XP_006711873.1:n.774-196_774-194delinsCTT
XR_949152.1:n.1055-196_1055-194delinsCTT
XM_006711802.3:c.774-196_774-194delinsCTT	XP_006711865.1:n.774-196_774-194delinsCTT
XM_006711803.3:c.774-196_774-194delinsCTT	XP_006711866.1:n.774-196_774-194delinsCTT
XM_006711804.3:c.774-196_774-194delinsCTT	XP_006711867.1:n.774-196_774-194delinsCTT
XM_006711805.3:c.774-196_774-194delinsCTT	XP_006711868.1:n.774-196_774-194delinsCTT
XM_006711806.3:c.774-196_774-194delinsCTT	XP_006711869.1:n.774-196_774-194delinsCTT
XM_006711807.3:c.774-196_774-194delinsCTT	XP_006711870.1:n.774-196_774-194delinsCTT
XM_006711808.3:c.774-196_774-194delinsCTT	XP_006711871.1:n.774-196_774-194delinsCTT
XM_006711810.3:c.774-196_774-194delinsCTT	XP_006711873.1:n.774-196_774-194delinsCTT
XM_017002028.1:c.753-196_753-194delinsCTT	XP_016857517.1:n.753-196_753-194delinsCTT
XR_002957299.1:n.1088-196_1088-194delinsCTT
XR_949152.2:n.1088-196_1088-194delinsCTT
NM_001035.3:c.774-196_774-194delinsCTT MANE Select	NP_001026.2:n.774-196_774-194delinsCTT