Canonical Allele Identifier: CA1148280428

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237640946A= , CM000663.2:g.237640946A=	GRCh38
NC_000001.10:g.237804246A= , CM000663.1:g.237804246A=	GRCh37
NC_000001.9:g.235870869A=	NCBI36
NG_008799.2:g.603545A=
NG_008799.3:g.603763A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.7165A=	ENSP00000499659.2:p.Met2389=
ENST00000659194.3:c.7165A=	ENSP00000499653.3:p.Met2389=
ENST00000660292.2:c.7165A=	ENSP00000499787.2:p.Met2389=
ENST00000366574.7:c.7165A= MANE Select	ENSP00000355533.2:p.Met2389=
ENST00000360064.7:c.7117A=	ENSP00000353174.7:p.Met2373=
ENST00000366574.6:c.7165A=	ENSP00000355533.2:p.Met2389=
NM_001035.2:c.7165A=	NP_001026.2:p.Met2389=
XM_006711802.2:c.7195A=	XP_006711865.1:p.Met2399=
XM_006711803.2:c.7192A=	XP_006711866.1:p.Met2398=
XM_006711804.2:c.7195A=	XP_006711867.1:p.Met2399=
XM_006711805.2:c.7165A=	XP_006711868.1:p.Met2389=
XM_006711806.2:c.7195A=	XP_006711869.1:p.Met2399=
XM_006711807.2:c.7195A=	XP_006711870.1:p.Met2399=
XM_006711808.2:c.7195A=	XP_006711871.1:p.Met2399=
XM_006711809.2:c.7195A=	XP_006711872.1:p.Met2399=
XM_006711810.2:c.7162A=	XP_006711873.1:p.Met2388=
XR_949152.1:n.7476A=
XM_006711802.3:c.7195A=	XP_006711865.1:p.Met2399=
XM_006711803.3:c.7192A=	XP_006711866.1:p.Met2398=
XM_006711804.3:c.7195A=	XP_006711867.1:p.Met2399=
XM_006711805.3:c.7165A=	XP_006711868.1:p.Met2389=
XM_006711806.3:c.7195A=	XP_006711869.1:p.Met2399=
XM_006711807.3:c.7195A=	XP_006711870.1:p.Met2399=
XM_006711808.3:c.7195A=	XP_006711871.1:p.Met2399=
XM_006711810.3:c.7162A=	XP_006711873.1:p.Met2388=
XM_017002028.1:c.7174A=	XP_016857517.1:p.Met2392=
XR_002957299.1:n.7509A=
XR_949152.2:n.7509A=
NM_001035.3:c.7165A= MANE Select	NP_001026.2:p.Met2389=