Canonical Allele Identifier: CA2487327695
Gene: RYR2 HGNC NCBI

Linked Data

dbSNP Id: rs1705046202

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237416804_237416807del , CM000663.2:g.237416804_237416807del GRCh38
NC_000001.10:g.237580104_237580107del , CM000663.1:g.237580104_237580107del GRCh37
NC_000001.9:g.235646727_235646730del NCBI36
NG_008799.2:g.379403_379406del
NG_008799.3:g.379621_379624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.774-245_774-242del ENSP00000499659.2:n.774-245_774-242del
ENST00000659194.3:c.774-245_774-242del ENSP00000499653.3:n.774-245_774-242del
ENST00000660292.2:c.774-245_774-242del ENSP00000499787.2:n.774-245_774-242del
ENST00000366574.7:c.774-245_774-242del MANE Select ENSP00000355533.2:n.774-245_774-242del
ENST00000360064.7:c.726-245_726-242del ENSP00000353174.7:n.726-245_726-242del
ENST00000366574.6:c.774-245_774-242del ENSP00000355533.2:n.774-245_774-242del
NM_001035.2:c.774-245_774-242del NP_001026.2:n.774-245_774-242del
XM_006711802.2:c.774-245_774-242del XP_006711865.1:n.774-245_774-242del
XM_006711803.2:c.774-245_774-242del XP_006711866.1:n.774-245_774-242del
XM_006711804.2:c.774-245_774-242del XP_006711867.1:n.774-245_774-242del
XM_006711805.2:c.774-245_774-242del XP_006711868.1:n.774-245_774-242del
XM_006711806.2:c.774-245_774-242del XP_006711869.1:n.774-245_774-242del
XM_006711807.2:c.774-245_774-242del XP_006711870.1:n.774-245_774-242del
XM_006711808.2:c.774-245_774-242del XP_006711871.1:n.774-245_774-242del
XM_006711809.2:c.774-245_774-242del XP_006711872.1:n.774-245_774-242del
XM_006711810.2:c.774-245_774-242del XP_006711873.1:n.774-245_774-242del
XR_949152.1:n.1055-245_1055-242del
XM_006711802.3:c.774-245_774-242del XP_006711865.1:n.774-245_774-242del
XM_006711803.3:c.774-245_774-242del XP_006711866.1:n.774-245_774-242del
XM_006711804.3:c.774-245_774-242del XP_006711867.1:n.774-245_774-242del
XM_006711805.3:c.774-245_774-242del XP_006711868.1:n.774-245_774-242del
XM_006711806.3:c.774-245_774-242del XP_006711869.1:n.774-245_774-242del
XM_006711807.3:c.774-245_774-242del XP_006711870.1:n.774-245_774-242del
XM_006711808.3:c.774-245_774-242del XP_006711871.1:n.774-245_774-242del
XM_006711810.3:c.774-245_774-242del XP_006711873.1:n.774-245_774-242del
XM_017002028.1:c.753-245_753-242del XP_016857517.1:n.753-245_753-242del
XR_002957299.1:n.1088-245_1088-242del
XR_949152.2:n.1088-245_1088-242del
NM_001035.3:c.774-245_774-242del MANE Select NP_001026.2:n.774-245_774-242del