Canonical Allele Identifier: CA086679

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237602087C>T , CM000663.2:g.237602087C>T	GRCh38
NC_000001.10:g.237765387C>T , CM000663.1:g.237765387C>T	GRCh37
NC_000001.9:g.235832010C>T	NCBI36
NG_008799.2:g.564686C>T
NG_008799.3:g.564904C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.4659C>T MANE Select	NP_001026.2:p.Phe1553=
ENST00000366574.7:c.4659C>T MANE Select	ENSP00000355533.2:p.Phe1553=
NM_001035.2:c.4659C>T	NP_001026.2:p.Phe1553=
ENST00000360064.7:c.4611C>T	ENSP00000353174.7:p.Phe1537=
ENST00000366574.6:c.4659C>T	ENSP00000355533.2:p.Phe1553=
ENST00000609119.2:c.4659C>T	ENSP00000499659.2:p.Phe1553=
ENST00000659194.3:c.4659C>T	ENSP00000499653.3:p.Phe1553=
ENST00000660292.2:c.4659C>T	ENSP00000499787.2:p.Phe1553=
XM_006711802.2:c.4689C>T	XP_006711865.1:p.Phe1563=
XM_006711802.3:c.4689C>T	XP_006711865.1:p.Phe1563=
XM_006711803.2:c.4686C>T	XP_006711866.1:p.Phe1562=
XM_006711803.3:c.4686C>T	XP_006711866.1:p.Phe1562=
XM_006711804.2:c.4689C>T	XP_006711867.1:p.Phe1563=
XM_006711804.3:c.4689C>T	XP_006711867.1:p.Phe1563=
XM_006711805.2:c.4659C>T	XP_006711868.1:p.Phe1553=
XM_006711805.3:c.4659C>T	XP_006711868.1:p.Phe1553=
XM_006711806.2:c.4689C>T	XP_006711869.1:p.Phe1563=
XM_006711806.3:c.4689C>T	XP_006711869.1:p.Phe1563=
XM_006711807.2:c.4689C>T	XP_006711870.1:p.Phe1563=
XM_006711807.3:c.4689C>T	XP_006711870.1:p.Phe1563=
XM_006711808.2:c.4689C>T	XP_006711871.1:p.Phe1563=
XM_006711808.3:c.4689C>T	XP_006711871.1:p.Phe1563=
XM_006711809.2:c.4689C>T	XP_006711872.1:p.Phe1563=
XM_006711810.2:c.4656C>T	XP_006711873.1:p.Phe1552=
XM_006711810.3:c.4656C>T	XP_006711873.1:p.Phe1552=
XM_017002028.1:c.4668C>T	XP_016857517.1:p.Phe1556=
XR_002957299.1:n.5003C>T
XR_949152.1:n.4970C>T
XR_949152.2:n.5003C>T