Canonical Allele Identifier: CA2651218615
Gene: RYR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237770740_237770744del , CM000663.2:g.237770740_237770744del GRCh38
NC_000001.10:g.237934040_237934044del , CM000663.1:g.237934040_237934044del GRCh37
NC_000001.9:g.236000663_236000667del NCBI36
NG_008799.2:g.733339_733343del
NG_008799.3:g.733557_733561del

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.*2569-67_*2569-63del ENSP00000499659.2:n.*2569-67_*2569-63del
ENST00000659194.3:c.11465-67_11465-63del ENSP00000499653.3:n.11465-67_11465-63del
ENST00000660292.2:c.11498-67_11498-63del ENSP00000499787.2:n.11498-67_11498-63del
ENST00000659194.2:c.3654-67_3654-63del
ENST00000366574.7:c.11477-67_11477-63del MANE Select ENSP00000355533.2:n.11477-67_11477-63del
ENST00000659194.1:c.3654-67_3654-63del
ENST00000660292.1:c.1530-67_1530-63del
ENST00000360064.7:c.11429-67_11429-63del ENSP00000353174.7:n.11429-67_11429-63del
ENST00000366574.6:c.11477-67_11477-63del ENSP00000355533.2:n.11477-67_11477-63del
ENST00000609119.1:n.2672-67_2672-63del
NM_001035.2:c.11477-67_11477-63del NP_001026.2:n.11477-67_11477-63del
XM_006711802.2:c.11531-67_11531-63del XP_006711865.1:n.11531-67_11531-63del
XM_006711803.2:c.11528-67_11528-63del XP_006711866.1:n.11528-67_11528-63del
XM_006711804.2:c.11507-67_11507-63del XP_006711867.1:n.11507-67_11507-63del
XM_006711805.2:c.11501-67_11501-63del XP_006711868.1:n.11501-67_11501-63del
XM_006711806.2:c.11495-67_11495-63del XP_006711869.1:n.11495-67_11495-63del
XM_006711807.2:c.11471-67_11471-63del XP_006711870.1:n.11471-67_11471-63del
XM_006711808.2:c.11294-67_11294-63del XP_006711871.1:n.11294-67_11294-63del
XM_006711810.2:c.11438-67_11438-63del XP_006711873.1:n.11438-67_11438-63del
XM_006711802.3:c.11531-67_11531-63del XP_006711865.1:n.11531-67_11531-63del
XM_006711803.3:c.11528-67_11528-63del XP_006711866.1:n.11528-67_11528-63del
XM_006711804.3:c.11507-67_11507-63del XP_006711867.1:n.11507-67_11507-63del
XM_006711805.3:c.11501-67_11501-63del XP_006711868.1:n.11501-67_11501-63del
XM_006711806.3:c.11495-67_11495-63del XP_006711869.1:n.11495-67_11495-63del
XM_006711807.3:c.11471-67_11471-63del XP_006711870.1:n.11471-67_11471-63del
XM_006711808.3:c.11294-67_11294-63del XP_006711871.1:n.11294-67_11294-63del
XM_006711810.3:c.11438-67_11438-63del XP_006711873.1:n.11438-67_11438-63del
XM_017002028.1:c.11510-67_11510-63del XP_016857517.1:n.11510-67_11510-63del
NM_001035.3:c.11477-67_11477-63del MANE Select NP_001026.2:n.11477-67_11477-63del