Canonical Allele Identifier: CA2573132870

Gene: RYR2

Linked Data

• ClinVar Variation Id: 1572434
• ClinVar RCV Id: RCV003006983
• dbSNP Id: rs2149314509

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237772008del , CM000663.2:g.237772008del	GRCh38
NC_000001.10:g.237935308del , CM000663.1:g.237935308del	GRCh37
NC_000001.9:g.236001931del	NCBI36
NG_008799.2:g.734607del
NG_008799.3:g.734825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*2650-4del	ENSP00000499659.2:n.*2650-4del
ENST00000659194.3:c.11546-4del	ENSP00000499653.3:n.11546-4del
ENST00000660292.2:c.11579-4del	ENSP00000499787.2:n.11579-4del
ENST00000659194.2:c.3735-4del
ENST00000366574.7:c.11558-4del MANE Select	ENSP00000355533.2:n.11558-4del
ENST00000659194.1:c.3735-4del
ENST00000660292.1:c.1611-4del
ENST00000360064.7:c.11510-4del	ENSP00000353174.7:n.11510-4del
ENST00000366574.6:c.11558-4del	ENSP00000355533.2:n.11558-4del
ENST00000609119.1:n.2753-4del
NM_001035.2:c.11558-4del	NP_001026.2:n.11558-4del
XM_006711802.2:c.11612-4del	XP_006711865.1:n.11612-4del
XM_006711803.2:c.11609-4del	XP_006711866.1:n.11609-4del
XM_006711804.2:c.11588-4del	XP_006711867.1:n.11588-4del
XM_006711805.2:c.11582-4del	XP_006711868.1:n.11582-4del
XM_006711806.2:c.11576-4del	XP_006711869.1:n.11576-4del
XM_006711807.2:c.11552-4del	XP_006711870.1:n.11552-4del
XM_006711808.2:c.11375-4del	XP_006711871.1:n.11375-4del
XM_006711810.2:c.11519-4del	XP_006711873.1:n.11519-4del
XM_006711802.3:c.11612-4del	XP_006711865.1:n.11612-4del
XM_006711803.3:c.11609-4del	XP_006711866.1:n.11609-4del
XM_006711804.3:c.11588-4del	XP_006711867.1:n.11588-4del
XM_006711805.3:c.11582-4del	XP_006711868.1:n.11582-4del
XM_006711806.3:c.11576-4del	XP_006711869.1:n.11576-4del
XM_006711807.3:c.11552-4del	XP_006711870.1:n.11552-4del
XM_006711808.3:c.11375-4del	XP_006711871.1:n.11375-4del
XM_006711810.3:c.11519-4del	XP_006711873.1:n.11519-4del
XM_017002028.1:c.11591-4del	XP_016857517.1:n.11591-4del
NM_001035.3:c.11558-4del MANE Select	NP_001026.2:n.11558-4del