Canonical Allele Identifier: CA1144083763

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237678117A= , CM000663.2:g.237678117A=	GRCh38
NC_000001.10:g.237841417A= , CM000663.1:g.237841417A=	GRCh37
NC_000001.9:g.235908040A=	NCBI36
NG_008799.2:g.640716A=
NG_008799.3:g.640934A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.8831-2339A=	ENSP00000499659.2:n.8831-2339A=
ENST00000659194.3:c.8895+5A=	ENSP00000499653.3:n.8895+5A=
ENST00000660292.2:c.8895+5A=	ENSP00000499787.2:n.8895+5A=
ENST00000659194.2:c.1084+5A=
ENST00000366574.7:c.8895+5A= MANE Select	ENSP00000355533.2:n.8895+5A=
ENST00000659194.1:c.1084+5A=
ENST00000360064.7:c.8847+5A=	ENSP00000353174.7:n.8847+5A=
ENST00000366574.6:c.8895+5A=	ENSP00000355533.2:n.8895+5A=
ENST00000609119.1:n.84-2339A=
NM_001035.2:c.8895+5A=	NP_001026.2:n.8895+5A=
XM_006711802.2:c.8925+5A=	XP_006711865.1:n.8925+5A=
XM_006711803.2:c.8922+5A=	XP_006711866.1:n.8922+5A=
XM_006711804.2:c.8925+5A=	XP_006711867.1:n.8925+5A=
XM_006711805.2:c.8895+5A=	XP_006711868.1:n.8895+5A=
XM_006711806.2:c.8925+5A=	XP_006711869.1:n.8925+5A=
XM_006711807.2:c.8925+5A=	XP_006711870.1:n.8925+5A=
XM_006711808.2:c.8860+3271A=	XP_006711871.1:n.8860+3271A=
XM_006711810.2:c.8892+5A=	XP_006711873.1:n.8892+5A=
XR_949152.1:n.9206+5A=
XM_006711802.3:c.8925+5A=	XP_006711865.1:n.8925+5A=
XM_006711803.3:c.8922+5A=	XP_006711866.1:n.8922+5A=
XM_006711804.3:c.8925+5A=	XP_006711867.1:n.8925+5A=
XM_006711805.3:c.8895+5A=	XP_006711868.1:n.8895+5A=
XM_006711806.3:c.8925+5A=	XP_006711869.1:n.8925+5A=
XM_006711807.3:c.8925+5A=	XP_006711870.1:n.8925+5A=
XM_006711808.3:c.8860+3271A=	XP_006711871.1:n.8860+3271A=
XM_006711810.3:c.8892+5A=	XP_006711873.1:n.8892+5A=
XM_017002028.1:c.8904+5A=	XP_016857517.1:n.8904+5A=
XR_949152.2:n.9239+5A=
NM_001035.3:c.8895+5A= MANE Select	NP_001026.2:n.8895+5A=