Canonical Allele Identifier: CA2487493340

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237808825C= , CM000663.2:g.237808825C=	GRCh38
NC_000001.10:g.237972125C= , CM000663.1:g.237972125C=	GRCh37
NC_000001.9:g.236038748C=	NCBI36
NG_008799.2:g.771424C=
NG_008799.3:g.771642C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5391-76C=	ENSP00000499659.2:n.*5391-76C=
ENST00000659194.3:c.14281-76C=	ENSP00000499653.3:n.14281-76C=
ENST00000660292.2:c.14320-76C=	ENSP00000499787.2:n.14320-76C=
ENST00000659194.2:c.6470-76C=
ENST00000366574.7:c.14299-76C= MANE Select	ENSP00000355533.2:n.14299-76C=
ENST00000360064.7:c.14248-76C=	ENSP00000353174.7:n.14248-76C=
ENST00000366574.6:c.14299-76C=	ENSP00000355533.2:n.14299-76C=
ENST00000608590.5:n.810-76C=
NM_001035.2:c.14299-76C=	NP_001026.2:n.14299-76C=
XM_006711802.2:c.14353-76C=	XP_006711865.1:n.14353-76C=
XM_006711803.2:c.14350-76C=	XP_006711866.1:n.14350-76C=
XM_006711804.2:c.14329-76C=	XP_006711867.1:n.14329-76C=
XM_006711805.2:c.14323-76C=	XP_006711868.1:n.14323-76C=
XM_006711806.2:c.14317-76C=	XP_006711869.1:n.14317-76C=
XM_006711807.2:c.14293-76C=	XP_006711870.1:n.14293-76C=
XM_006711808.2:c.14116-76C=	XP_006711871.1:n.14116-76C=
XM_006711810.2:c.14260-76C=	XP_006711873.1:n.14260-76C=
XM_006711802.3:c.14353-76C=	XP_006711865.1:n.14353-76C=
XM_006711803.3:c.14350-76C=	XP_006711866.1:n.14350-76C=
XM_006711804.3:c.14329-76C=	XP_006711867.1:n.14329-76C=
XM_006711805.3:c.14323-76C=	XP_006711868.1:n.14323-76C=
XM_006711806.3:c.14317-76C=	XP_006711869.1:n.14317-76C=
XM_006711807.3:c.14293-76C=	XP_006711870.1:n.14293-76C=
XM_006711808.3:c.14116-76C=	XP_006711871.1:n.14116-76C=
XM_006711810.3:c.14260-76C=	XP_006711873.1:n.14260-76C=
XM_017002028.1:c.14332-76C=	XP_016857517.1:n.14332-76C=
NM_001035.3:c.14299-76C= MANE Select	NP_001026.2:n.14299-76C=