Canonical Allele Identifier: CA2825000952

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237674850G>C , CM000663.2:g.237674850G>C	GRCh38
NC_000001.10:g.237838150G>C , CM000663.1:g.237838150G>C	GRCh37
NC_000001.9:g.235904773G>C	NCBI36
NG_008799.2:g.637449G>C
NG_008799.3:g.637667G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.8830+4G>C MANE Select	NP_001026.2:n.8830+4G>C
ENST00000366574.7:c.8830+4G>C MANE Select	ENSP00000355533.2:n.8830+4G>C
NM_001035.2:c.8830+4G>C	NP_001026.2:n.8830+4G>C
ENST00000360064.7:c.8782+4G>C	ENSP00000353174.7:n.8782+4G>C
ENST00000366574.6:c.8830+4G>C	ENSP00000355533.2:n.8830+4G>C
ENST00000609119.1:n.83+4G>C
ENST00000609119.2:c.8830+4G>C	ENSP00000499659.2:n.8830+4G>C
ENST00000659194.1:c.1019+4G>C
ENST00000659194.2:c.1019+4G>C
ENST00000659194.3:c.8830+4G>C	ENSP00000499653.3:n.8830+4G>C
ENST00000660292.2:c.8830+4G>C	ENSP00000499787.2:n.8830+4G>C
XM_006711802.2:c.8860+4G>C	XP_006711865.1:n.8860+4G>C
XM_006711802.3:c.8860+4G>C	XP_006711865.1:n.8860+4G>C
XM_006711803.2:c.8857+4G>C	XP_006711866.1:n.8857+4G>C
XM_006711803.3:c.8857+4G>C	XP_006711866.1:n.8857+4G>C
XM_006711804.2:c.8860+4G>C	XP_006711867.1:n.8860+4G>C
XM_006711804.3:c.8860+4G>C	XP_006711867.1:n.8860+4G>C
XM_006711805.2:c.8830+4G>C	XP_006711868.1:n.8830+4G>C
XM_006711805.3:c.8830+4G>C	XP_006711868.1:n.8830+4G>C
XM_006711806.2:c.8860+4G>C	XP_006711869.1:n.8860+4G>C
XM_006711806.3:c.8860+4G>C	XP_006711869.1:n.8860+4G>C
XM_006711807.2:c.8860+4G>C	XP_006711870.1:n.8860+4G>C
XM_006711807.3:c.8860+4G>C	XP_006711870.1:n.8860+4G>C
XM_006711808.2:c.8860+4G>C	XP_006711871.1:n.8860+4G>C
XM_006711808.3:c.8860+4G>C	XP_006711871.1:n.8860+4G>C
XM_006711810.2:c.8827+4G>C	XP_006711873.1:n.8827+4G>C
XM_006711810.3:c.8827+4G>C	XP_006711873.1:n.8827+4G>C
XM_017002028.1:c.8839+4G>C	XP_016857517.1:n.8839+4G>C
XR_949152.1:n.9141+4G>C
XR_949152.2:n.9174+4G>C