Canonical Allele Identifier: CA1145848156

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237627972T= , CM000663.2:g.237627972T=	GRCh38
NC_000001.10:g.237791272T= , CM000663.1:g.237791272T=	GRCh37
NC_000001.9:g.235857895T=	NCBI36
NG_008799.2:g.590571T=
NG_008799.3:g.590789T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.6332T=	ENSP00000499659.2:p.Val2111=
ENST00000659194.3:c.6332T=	ENSP00000499653.3:p.Val2111=
ENST00000660292.2:c.6332T=	ENSP00000499787.2:p.Val2111=
ENST00000366574.7:c.6332T= MANE Select	ENSP00000355533.2:p.Val2111=
ENST00000360064.7:c.6284T=	ENSP00000353174.7:p.Val2095=
ENST00000366574.6:c.6332T=	ENSP00000355533.2:p.Val2111=
NM_001035.2:c.6332T=	NP_001026.2:p.Val2111=
XM_006711802.2:c.6362T=	XP_006711865.1:p.Val2121=
XM_006711803.2:c.6359T=	XP_006711866.1:p.Val2120=
XM_006711804.2:c.6362T=	XP_006711867.1:p.Val2121=
XM_006711805.2:c.6332T=	XP_006711868.1:p.Val2111=
XM_006711806.2:c.6362T=	XP_006711869.1:p.Val2121=
XM_006711807.2:c.6362T=	XP_006711870.1:p.Val2121=
XM_006711808.2:c.6362T=	XP_006711871.1:p.Val2121=
XM_006711809.2:c.6362T=	XP_006711872.1:p.Val2121=
XM_006711810.2:c.6329T=	XP_006711873.1:p.Val2110=
XR_949152.1:n.6643T=
XM_006711802.3:c.6362T=	XP_006711865.1:p.Val2121=
XM_006711803.3:c.6359T=	XP_006711866.1:p.Val2120=
XM_006711804.3:c.6362T=	XP_006711867.1:p.Val2121=
XM_006711805.3:c.6332T=	XP_006711868.1:p.Val2111=
XM_006711806.3:c.6362T=	XP_006711869.1:p.Val2121=
XM_006711807.3:c.6362T=	XP_006711870.1:p.Val2121=
XM_006711808.3:c.6362T=	XP_006711871.1:p.Val2121=
XM_006711810.3:c.6329T=	XP_006711873.1:p.Val2110=
XM_017002028.1:c.6341T=	XP_016857517.1:p.Val2114=
XR_002957299.1:n.6676T=
XR_949152.2:n.6676T=
NM_001035.3:c.6332T= MANE Select	NP_001026.2:p.Val2111=