Canonical Allele Identifier: CA345413413

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947485C>T (hg19) ; chr1:g.237784185C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784185C>T , CM000663.2:g.237784185C>T	GRCh38
NC_000001.10:g.237947485C>T , CM000663.1:g.237947485C>T	GRCh37
NC_000001.9:g.236014108C>T	NCBI36
NG_008799.2:g.746784C>T
NG_008799.3:g.747002C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3565C>T	ENSP00000499659.2:n.*3565C>T
ENST00000659194.3:c.12461C>T	ENSP00000499653.3:p.Thr4154Ile
ENST00000660292.2:c.12494C>T	ENSP00000499787.2:p.Thr4165Ile
ENST00000659194.2:c.4650C>T
ENST00000366574.7:c.12473C>T MANE Select	ENSP00000355533.2:p.Thr4158Ile
ENST00000659194.1:c.4650C>T
ENST00000660292.1:c.2526C>T
ENST00000360064.7:c.12425C>T	ENSP00000353174.7:p.Thr4142Ile
ENST00000366574.6:c.12473C>T	ENSP00000355533.2:p.Thr4158Ile
ENST00000609119.1:n.3668C>T
NM_001035.2:c.12473C>T	NP_001026.2:p.Thr4158Ile
XM_006711802.2:c.12527C>T	XP_006711865.1:p.Thr4176Ile
XM_006711803.2:c.12524C>T	XP_006711866.1:p.Thr4175Ile
XM_006711804.2:c.12503C>T	XP_006711867.1:p.Thr4168Ile
XM_006711805.2:c.12497C>T	XP_006711868.1:p.Thr4166Ile
XM_006711806.2:c.12491C>T	XP_006711869.1:p.Thr4164Ile
XM_006711807.2:c.12467C>T	XP_006711870.1:p.Thr4156Ile
XM_006711808.2:c.12290C>T	XP_006711871.1:p.Thr4097Ile
XM_006711810.2:c.12434C>T	XP_006711873.1:p.Thr4145Ile
XM_006711802.3:c.12527C>T	XP_006711865.1:p.Thr4176Ile
XM_006711803.3:c.12524C>T	XP_006711866.1:p.Thr4175Ile
XM_006711804.3:c.12503C>T	XP_006711867.1:p.Thr4168Ile
XM_006711805.3:c.12497C>T	XP_006711868.1:p.Thr4166Ile
XM_006711806.3:c.12491C>T	XP_006711869.1:p.Thr4164Ile
XM_006711807.3:c.12467C>T	XP_006711870.1:p.Thr4156Ile
XM_006711808.3:c.12290C>T	XP_006711871.1:p.Thr4097Ile
XM_006711810.3:c.12434C>T	XP_006711873.1:p.Thr4145Ile
XM_017002028.1:c.12506C>T	XP_016857517.1:p.Thr4169Ile
NM_001035.3:c.12473C>T MANE Select	NP_001026.2:p.Thr4158Ile