Canonical Allele Identifier: CA2487493396

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237808974A= , CM000663.2:g.237808974A=	GRCh38
NC_000001.10:g.237972274A= , CM000663.1:g.237972274A=	GRCh37
NC_000001.9:g.236038897A=	NCBI36
NG_008799.2:g.771573A=
NG_008799.3:g.771791A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5464A=	ENSP00000499659.2:n.*5464A=
ENST00000659194.3:c.14354A=	ENSP00000499653.3:p.Lys4785=
ENST00000660292.2:c.14393A=	ENSP00000499787.2:p.Lys4798=
ENST00000659194.2:c.6543A=
ENST00000366574.7:c.14372A= MANE Select	ENSP00000355533.2:p.Lys4791=
ENST00000360064.7:c.14321A=	ENSP00000353174.7:p.Lys4774=
ENST00000366574.6:c.14372A=	ENSP00000355533.2:p.Lys4791=
ENST00000608590.5:n.883A=
NM_001035.2:c.14372A=	NP_001026.2:p.Lys4791=
XM_006711802.2:c.14426A=	XP_006711865.1:p.Lys4809=
XM_006711803.2:c.14423A=	XP_006711866.1:p.Lys4808=
XM_006711804.2:c.14402A=	XP_006711867.1:p.Lys4801=
XM_006711805.2:c.14396A=	XP_006711868.1:p.Lys4799=
XM_006711806.2:c.14390A=	XP_006711869.1:p.Lys4797=
XM_006711807.2:c.14366A=	XP_006711870.1:p.Lys4789=
XM_006711808.2:c.14189A=	XP_006711871.1:p.Lys4730=
XM_006711810.2:c.14333A=	XP_006711873.1:p.Lys4778=
XM_006711802.3:c.14426A=	XP_006711865.1:p.Lys4809=
XM_006711803.3:c.14423A=	XP_006711866.1:p.Lys4808=
XM_006711804.3:c.14402A=	XP_006711867.1:p.Lys4801=
XM_006711805.3:c.14396A=	XP_006711868.1:p.Lys4799=
XM_006711806.3:c.14390A=	XP_006711869.1:p.Lys4797=
XM_006711807.3:c.14366A=	XP_006711870.1:p.Lys4789=
XM_006711808.3:c.14189A=	XP_006711871.1:p.Lys4730=
XM_006711810.3:c.14333A=	XP_006711873.1:p.Lys4778=
XM_017002028.1:c.14405A=	XP_016857517.1:p.Lys4802=
NM_001035.3:c.14372A= MANE Select	NP_001026.2:p.Lys4791=