Canonical Allele Identifier: CA424031697

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237870370C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237707070C>T , CM000663.2:g.237707070C>T	GRCh38
NC_000001.10:g.237870370C>T , CM000663.1:g.237870370C>T	GRCh37
NC_000001.9:g.235936993C>T	NCBI36
NG_008799.2:g.669669C>T
NG_008799.3:g.669887C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*737C>T	ENSP00000499659.2:n.*737C>T
ENST00000659194.3:c.9702C>T	ENSP00000499653.3:p.Val3234=
ENST00000660292.2:c.9702C>T	ENSP00000499787.2:p.Val3234=
ENST00000659194.2:c.1891C>T
ENST00000366574.7:c.9702C>T MANE Select	ENSP00000355533.2:p.Val3234=
ENST00000659194.1:c.1891C>T
ENST00000360064.7:c.9654C>T	ENSP00000353174.7:p.Val3218=
ENST00000366574.6:c.9702C>T	ENSP00000355533.2:p.Val3234=
ENST00000609119.1:n.840C>T
NM_001035.2:c.9702C>T	NP_001026.2:p.Val3234=
XM_006711802.2:c.9732C>T	XP_006711865.1:p.Val3244=
XM_006711803.2:c.9729C>T	XP_006711866.1:p.Val3243=
XM_006711804.2:c.9732C>T	XP_006711867.1:p.Val3244=
XM_006711805.2:c.9702C>T	XP_006711868.1:p.Val3234=
XM_006711806.2:c.9732C>T	XP_006711869.1:p.Val3244=
XM_006711807.2:c.9732C>T	XP_006711870.1:p.Val3244=
XM_006711808.2:c.9495C>T	XP_006711871.1:p.Val3165=
XM_006711810.2:c.9699C>T	XP_006711873.1:p.Val3233=
XM_006711802.3:c.9732C>T	XP_006711865.1:p.Val3244=
XM_006711803.3:c.9729C>T	XP_006711866.1:p.Val3243=
XM_006711804.3:c.9732C>T	XP_006711867.1:p.Val3244=
XM_006711805.3:c.9702C>T	XP_006711868.1:p.Val3234=
XM_006711806.3:c.9732C>T	XP_006711869.1:p.Val3244=
XM_006711807.3:c.9732C>T	XP_006711870.1:p.Val3244=
XM_006711808.3:c.9495C>T	XP_006711871.1:p.Val3165=
XM_006711810.3:c.9699C>T	XP_006711873.1:p.Val3233=
XM_017002028.1:c.9711C>T	XP_016857517.1:p.Val3237=
NM_001035.3:c.9702C>T MANE Select	NP_001026.2:p.Val3234=