Canonical Allele Identifier: CA2487327698

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237416812_237416813delinsCA , CM000663.2:g.237416812_237416813delinsCA	GRCh38
NC_000001.10:g.237580112_237580113delinsCA , CM000663.1:g.237580112_237580113delinsCA	GRCh37
NC_000001.9:g.235646735_235646736delinsCA	NCBI36
NG_008799.2:g.379411_379412delinsCA
NG_008799.3:g.379629_379630delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.774-237_774-236delinsCA	ENSP00000499659.2:n.774-237_774-236delinsCA
ENST00000659194.3:c.774-237_774-236delinsCA	ENSP00000499653.3:n.774-237_774-236delinsCA
ENST00000660292.2:c.774-237_774-236delinsCA	ENSP00000499787.2:n.774-237_774-236delinsCA
ENST00000366574.7:c.774-237_774-236delinsCA MANE Select	ENSP00000355533.2:n.774-237_774-236delinsCA
ENST00000360064.7:c.726-237_726-236delinsCA	ENSP00000353174.7:n.726-237_726-236delinsCA
ENST00000366574.6:c.774-237_774-236delinsCA	ENSP00000355533.2:n.774-237_774-236delinsCA
NM_001035.2:c.774-237_774-236delinsCA	NP_001026.2:n.774-237_774-236delinsCA
XM_006711802.2:c.774-237_774-236delinsCA	XP_006711865.1:n.774-237_774-236delinsCA
XM_006711803.2:c.774-237_774-236delinsCA	XP_006711866.1:n.774-237_774-236delinsCA
XM_006711804.2:c.774-237_774-236delinsCA	XP_006711867.1:n.774-237_774-236delinsCA
XM_006711805.2:c.774-237_774-236delinsCA	XP_006711868.1:n.774-237_774-236delinsCA
XM_006711806.2:c.774-237_774-236delinsCA	XP_006711869.1:n.774-237_774-236delinsCA
XM_006711807.2:c.774-237_774-236delinsCA	XP_006711870.1:n.774-237_774-236delinsCA
XM_006711808.2:c.774-237_774-236delinsCA	XP_006711871.1:n.774-237_774-236delinsCA
XM_006711809.2:c.774-237_774-236delinsCA	XP_006711872.1:n.774-237_774-236delinsCA
XM_006711810.2:c.774-237_774-236delinsCA	XP_006711873.1:n.774-237_774-236delinsCA
XR_949152.1:n.1055-237_1055-236delinsCA
XM_006711802.3:c.774-237_774-236delinsCA	XP_006711865.1:n.774-237_774-236delinsCA
XM_006711803.3:c.774-237_774-236delinsCA	XP_006711866.1:n.774-237_774-236delinsCA
XM_006711804.3:c.774-237_774-236delinsCA	XP_006711867.1:n.774-237_774-236delinsCA
XM_006711805.3:c.774-237_774-236delinsCA	XP_006711868.1:n.774-237_774-236delinsCA
XM_006711806.3:c.774-237_774-236delinsCA	XP_006711869.1:n.774-237_774-236delinsCA
XM_006711807.3:c.774-237_774-236delinsCA	XP_006711870.1:n.774-237_774-236delinsCA
XM_006711808.3:c.774-237_774-236delinsCA	XP_006711871.1:n.774-237_774-236delinsCA
XM_006711810.3:c.774-237_774-236delinsCA	XP_006711873.1:n.774-237_774-236delinsCA
XM_017002028.1:c.753-237_753-236delinsCA	XP_016857517.1:n.753-237_753-236delinsCA
XR_002957299.1:n.1088-237_1088-236delinsCA
XR_949152.2:n.1088-237_1088-236delinsCA
NM_001035.3:c.774-237_774-236delinsCA MANE Select	NP_001026.2:n.774-237_774-236delinsCA