Canonical Allele Identifier: CA2487327664

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237416761_237416765delinsCACAG , CM000663.2:g.237416761_237416765delinsCACAG	GRCh38
NC_000001.10:g.237580061_237580065delinsCACAG , CM000663.1:g.237580061_237580065delinsCACAG	GRCh37
NC_000001.9:g.235646684_235646688delinsCACAG	NCBI36
NG_008799.2:g.379360_379364delinsCACAG
NG_008799.3:g.379578_379582delinsCACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.774-288_774-284delinsCACAG	ENSP00000499659.2:n.774-288_774-284delinsCACAG
ENST00000659194.3:c.774-288_774-284delinsCACAG	ENSP00000499653.3:n.774-288_774-284delinsCACAG
ENST00000660292.2:c.774-288_774-284delinsCACAG	ENSP00000499787.2:n.774-288_774-284delinsCACAG
ENST00000366574.7:c.774-288_774-284delinsCACAG MANE Select	ENSP00000355533.2:n.774-288_774-284delinsCACAG
ENST00000360064.7:c.726-288_726-284delinsCACAG	ENSP00000353174.7:n.726-288_726-284delinsCACAG
ENST00000366574.6:c.774-288_774-284delinsCACAG	ENSP00000355533.2:n.774-288_774-284delinsCACAG
NM_001035.2:c.774-288_774-284delinsCACAG	NP_001026.2:n.774-288_774-284delinsCACAG
XM_006711802.2:c.774-288_774-284delinsCACAG	XP_006711865.1:n.774-288_774-284delinsCACAG
XM_006711803.2:c.774-288_774-284delinsCACAG	XP_006711866.1:n.774-288_774-284delinsCACAG
XM_006711804.2:c.774-288_774-284delinsCACAG	XP_006711867.1:n.774-288_774-284delinsCACAG
XM_006711805.2:c.774-288_774-284delinsCACAG	XP_006711868.1:n.774-288_774-284delinsCACAG
XM_006711806.2:c.774-288_774-284delinsCACAG	XP_006711869.1:n.774-288_774-284delinsCACAG
XM_006711807.2:c.774-288_774-284delinsCACAG	XP_006711870.1:n.774-288_774-284delinsCACAG
XM_006711808.2:c.774-288_774-284delinsCACAG	XP_006711871.1:n.774-288_774-284delinsCACAG
XM_006711809.2:c.774-288_774-284delinsCACAG	XP_006711872.1:n.774-288_774-284delinsCACAG
XM_006711810.2:c.774-288_774-284delinsCACAG	XP_006711873.1:n.774-288_774-284delinsCACAG
XR_949152.1:n.1055-288_1055-284delinsCACAG
XM_006711802.3:c.774-288_774-284delinsCACAG	XP_006711865.1:n.774-288_774-284delinsCACAG
XM_006711803.3:c.774-288_774-284delinsCACAG	XP_006711866.1:n.774-288_774-284delinsCACAG
XM_006711804.3:c.774-288_774-284delinsCACAG	XP_006711867.1:n.774-288_774-284delinsCACAG
XM_006711805.3:c.774-288_774-284delinsCACAG	XP_006711868.1:n.774-288_774-284delinsCACAG
XM_006711806.3:c.774-288_774-284delinsCACAG	XP_006711869.1:n.774-288_774-284delinsCACAG
XM_006711807.3:c.774-288_774-284delinsCACAG	XP_006711870.1:n.774-288_774-284delinsCACAG
XM_006711808.3:c.774-288_774-284delinsCACAG	XP_006711871.1:n.774-288_774-284delinsCACAG
XM_006711810.3:c.774-288_774-284delinsCACAG	XP_006711873.1:n.774-288_774-284delinsCACAG
XM_017002028.1:c.753-288_753-284delinsCACAG	XP_016857517.1:n.753-288_753-284delinsCACAG
XR_002957299.1:n.1088-288_1088-284delinsCACAG
XR_949152.2:n.1088-288_1088-284delinsCACAG
NM_001035.3:c.774-288_774-284delinsCACAG MANE Select	NP_001026.2:n.774-288_774-284delinsCACAG