Canonical Allele Identifier: CA2651197876

Gene: RYR2

Linked Data

• gnomAD v4: 1-237417108-A-AGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237417110_237417112dup , CM000663.2:g.237417110_237417112dup	GRCh38
NC_000001.10:g.237580410_237580412dup , CM000663.1:g.237580410_237580412dup	GRCh37
NC_000001.9:g.235647033_235647035dup	NCBI36
NG_008799.2:g.379709_379711dup
NG_008799.3:g.379927_379929dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.835_837dup	ENSP00000499659.2:p.Thr279_Leu280insThr
ENST00000659194.3:c.835_837dup	ENSP00000499653.3:p.Thr279_Leu280insThr
ENST00000660292.2:c.835_837dup	ENSP00000499787.2:p.Thr279_Leu280insThr
ENST00000366574.7:c.835_837dup MANE Select	ENSP00000355533.2:p.Thr279_Leu280insThr
ENST00000360064.7:c.787_789dup	ENSP00000353174.7:p.Thr263_Leu264insThr
ENST00000366574.6:c.835_837dup	ENSP00000355533.2:p.Thr279_Leu280insThr
NM_001035.2:c.835_837dup	NP_001026.2:p.Thr279_Leu280insThr
XM_006711802.2:c.835_837dup	XP_006711865.1:p.Thr279_Leu280insThr
XM_006711803.2:c.835_837dup	XP_006711866.1:p.Thr279_Leu280insThr
XM_006711804.2:c.835_837dup	XP_006711867.1:p.Thr279_Leu280insThr
XM_006711805.2:c.835_837dup	XP_006711868.1:p.Thr279_Leu280insThr
XM_006711806.2:c.835_837dup	XP_006711869.1:p.Thr279_Leu280insThr
XM_006711807.2:c.835_837dup	XP_006711870.1:p.Thr279_Leu280insThr
XM_006711808.2:c.835_837dup	XP_006711871.1:p.Thr279_Leu280insThr
XM_006711809.2:c.835_837dup	XP_006711872.1:p.Thr279_Leu280insThr
XM_006711810.2:c.835_837dup	XP_006711873.1:p.Thr279_Leu280insThr
XR_949152.1:n.1116_1118dup
XM_006711802.3:c.835_837dup	XP_006711865.1:p.Thr279_Leu280insThr
XM_006711803.3:c.835_837dup	XP_006711866.1:p.Thr279_Leu280insThr
XM_006711804.3:c.835_837dup	XP_006711867.1:p.Thr279_Leu280insThr
XM_006711805.3:c.835_837dup	XP_006711868.1:p.Thr279_Leu280insThr
XM_006711806.3:c.835_837dup	XP_006711869.1:p.Thr279_Leu280insThr
XM_006711807.3:c.835_837dup	XP_006711870.1:p.Thr279_Leu280insThr
XM_006711808.3:c.835_837dup	XP_006711871.1:p.Thr279_Leu280insThr
XM_006711810.3:c.835_837dup	XP_006711873.1:p.Thr279_Leu280insThr
XM_017002028.1:c.814_816dup	XP_016857517.1:p.Thr272_Leu273insThr
XR_002957299.1:n.1149_1151dup
XR_949152.2:n.1149_1151dup
NM_001035.3:c.835_837dup MANE Select	NP_001026.2:p.Thr279_Leu280insThr