Canonical Allele Identifier: CA913187853

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237680583C>T , CM000663.2:g.237680583C>T	GRCh38
NC_000001.10:g.237843883C>T , CM000663.1:g.237843883C>T	GRCh37
NC_000001.9:g.235910506C>T	NCBI36
NG_008799.2:g.643182C>T
NG_008799.3:g.643400C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.9017+6C>T MANE Select	NP_001026.2:n.9017+6C>T
ENST00000366574.7:c.9017+6C>T MANE Select	ENSP00000355533.2:n.9017+6C>T
NM_001035.2:c.9017+6C>T	NP_001026.2:n.9017+6C>T
ENST00000360064.7:c.8969+6C>T	ENSP00000353174.7:n.8969+6C>T
ENST00000366574.6:c.9017+6C>T	ENSP00000355533.2:n.9017+6C>T
ENST00000609119.1:n.205+6C>T
ENST00000609119.2:c.*102+6C>T	ENSP00000499659.2:n.*102+6C>T
ENST00000659194.1:c.1206+6C>T
ENST00000659194.2:c.1206+6C>T
ENST00000659194.3:c.9017+6C>T	ENSP00000499653.3:n.9017+6C>T
ENST00000660292.2:c.9017+6C>T	ENSP00000499787.2:n.9017+6C>T
XM_006711802.2:c.9047+6C>T	XP_006711865.1:n.9047+6C>T
XM_006711802.3:c.9047+6C>T	XP_006711865.1:n.9047+6C>T
XM_006711803.2:c.9044+6C>T	XP_006711866.1:n.9044+6C>T
XM_006711803.3:c.9044+6C>T	XP_006711866.1:n.9044+6C>T
XM_006711804.2:c.9047+6C>T	XP_006711867.1:n.9047+6C>T
XM_006711804.3:c.9047+6C>T	XP_006711867.1:n.9047+6C>T
XM_006711805.2:c.9017+6C>T	XP_006711868.1:n.9017+6C>T
XM_006711805.3:c.9017+6C>T	XP_006711868.1:n.9017+6C>T
XM_006711806.2:c.9047+6C>T	XP_006711869.1:n.9047+6C>T
XM_006711806.3:c.9047+6C>T	XP_006711869.1:n.9047+6C>T
XM_006711807.2:c.9047+6C>T	XP_006711870.1:n.9047+6C>T
XM_006711807.3:c.9047+6C>T	XP_006711870.1:n.9047+6C>T
XM_006711808.2:c.8860+5737C>T	XP_006711871.1:n.8860+5737C>T
XM_006711808.3:c.8860+5737C>T	XP_006711871.1:n.8860+5737C>T
XM_006711810.2:c.9014+6C>T	XP_006711873.1:n.9014+6C>T
XM_006711810.3:c.9014+6C>T	XP_006711873.1:n.9014+6C>T
XM_017002028.1:c.9026+6C>T	XP_016857517.1:n.9026+6C>T
XR_949152.1:n.9328+6C>T
XR_949152.2:n.9361+6C>T