Canonical Allele Identifier: CA2487493249
Gene: RYR2 HGNC NCBI

Linked Data

dbSNP Id: rs1660912907

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237808653_237808654insAA , CM000663.2:g.237808653_237808654insAA GRCh38
NC_000001.10:g.237971953_237971954insAA , CM000663.1:g.237971953_237971954insAA GRCh37
NC_000001.9:g.236038576_236038577insAA NCBI36
NG_008799.2:g.771252_771253insAA
NG_008799.3:g.771470_771471insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.*5391-248_*5391-247insAA ENSP00000499659.2:n.*5391-248_*5391-247insAA
ENST00000659194.3:c.14281-248_14281-247insAA ENSP00000499653.3:n.14281-248_14281-247insAA
ENST00000660292.2:c.14320-248_14320-247insAA ENSP00000499787.2:n.14320-248_14320-247insAA
ENST00000659194.2:c.6470-248_6470-247insAA
ENST00000366574.7:c.14299-248_14299-247insAA MANE Select ENSP00000355533.2:n.14299-248_14299-247insAA
ENST00000360064.7:c.14248-248_14248-247insAA ENSP00000353174.7:n.14248-248_14248-247insAA
ENST00000366574.6:c.14299-248_14299-247insAA ENSP00000355533.2:n.14299-248_14299-247insAA
ENST00000608590.5:n.810-248_810-247insAA
NM_001035.2:c.14299-248_14299-247insAA NP_001026.2:n.14299-248_14299-247insAA
XM_006711802.2:c.14353-248_14353-247insAA XP_006711865.1:n.14353-248_14353-247insAA
XM_006711803.2:c.14350-248_14350-247insAA XP_006711866.1:n.14350-248_14350-247insAA
XM_006711804.2:c.14329-248_14329-247insAA XP_006711867.1:n.14329-248_14329-247insAA
XM_006711805.2:c.14323-248_14323-247insAA XP_006711868.1:n.14323-248_14323-247insAA
XM_006711806.2:c.14317-248_14317-247insAA XP_006711869.1:n.14317-248_14317-247insAA
XM_006711807.2:c.14293-248_14293-247insAA XP_006711870.1:n.14293-248_14293-247insAA
XM_006711808.2:c.14116-248_14116-247insAA XP_006711871.1:n.14116-248_14116-247insAA
XM_006711810.2:c.14260-248_14260-247insAA XP_006711873.1:n.14260-248_14260-247insAA
XM_006711802.3:c.14353-248_14353-247insAA XP_006711865.1:n.14353-248_14353-247insAA
XM_006711803.3:c.14350-248_14350-247insAA XP_006711866.1:n.14350-248_14350-247insAA
XM_006711804.3:c.14329-248_14329-247insAA XP_006711867.1:n.14329-248_14329-247insAA
XM_006711805.3:c.14323-248_14323-247insAA XP_006711868.1:n.14323-248_14323-247insAA
XM_006711806.3:c.14317-248_14317-247insAA XP_006711869.1:n.14317-248_14317-247insAA
XM_006711807.3:c.14293-248_14293-247insAA XP_006711870.1:n.14293-248_14293-247insAA
XM_006711808.3:c.14116-248_14116-247insAA XP_006711871.1:n.14116-248_14116-247insAA
XM_006711810.3:c.14260-248_14260-247insAA XP_006711873.1:n.14260-248_14260-247insAA
XM_017002028.1:c.14332-248_14332-247insAA XP_016857517.1:n.14332-248_14332-247insAA
NM_001035.3:c.14299-248_14299-247insAA MANE Select NP_001026.2:n.14299-248_14299-247insAA