Canonical Allele Identifier: CA345380471

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237454503C>T , CM000663.2:g.237454503C>T	GRCh38
NC_000001.10:g.237617803C>T , CM000663.1:g.237617803C>T	GRCh37
NC_000001.9:g.235684426C>T	NCBI36
NG_008799.2:g.417102C>T
NG_008799.3:g.417320C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.1405C>T MANE Select	NP_001026.2:p.His469Tyr
ENST00000366574.7:c.1405C>T MANE Select	ENSP00000355533.2:p.His469Tyr
NM_001035.2:c.1405C>T	NP_001026.2:p.His469Tyr
ENST00000360064.7:c.1357C>T	ENSP00000353174.7:p.His453Tyr
ENST00000366574.6:c.1405C>T	ENSP00000355533.2:p.His469Tyr
ENST00000609119.2:c.1405C>T	ENSP00000499659.2:p.His469Tyr
ENST00000659194.3:c.1405C>T	ENSP00000499653.3:p.His469Tyr
ENST00000660292.2:c.1405C>T	ENSP00000499787.2:p.His469Tyr
XM_006711802.2:c.1405C>T	XP_006711865.1:p.His469Tyr
XM_006711802.3:c.1405C>T	XP_006711865.1:p.His469Tyr
XM_006711803.2:c.1405C>T	XP_006711866.1:p.His469Tyr
XM_006711803.3:c.1405C>T	XP_006711866.1:p.His469Tyr
XM_006711804.2:c.1405C>T	XP_006711867.1:p.His469Tyr
XM_006711804.3:c.1405C>T	XP_006711867.1:p.His469Tyr
XM_006711805.2:c.1405C>T	XP_006711868.1:p.His469Tyr
XM_006711805.3:c.1405C>T	XP_006711868.1:p.His469Tyr
XM_006711806.2:c.1405C>T	XP_006711869.1:p.His469Tyr
XM_006711806.3:c.1405C>T	XP_006711869.1:p.His469Tyr
XM_006711807.2:c.1405C>T	XP_006711870.1:p.His469Tyr
XM_006711807.3:c.1405C>T	XP_006711870.1:p.His469Tyr
XM_006711808.2:c.1405C>T	XP_006711871.1:p.His469Tyr
XM_006711808.3:c.1405C>T	XP_006711871.1:p.His469Tyr
XM_006711809.2:c.1405C>T	XP_006711872.1:p.His469Tyr
XM_006711810.2:c.1405C>T	XP_006711873.1:p.His469Tyr
XM_006711810.3:c.1405C>T	XP_006711873.1:p.His469Tyr
XM_017002028.1:c.1384C>T	XP_016857517.1:p.His462Tyr
XR_002957299.1:n.1719C>T
XR_949152.1:n.1686C>T
XR_949152.2:n.1719C>T