Canonical Allele Identifier: CA916436351
Gene: RYR2 HGNC NCBI

Linked Data

dbSNP Id: rs35162950

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237808664_237808668dup , CM000663.2:g.237808664_237808668dup GRCh38
NC_000001.10:g.237971964_237971968dup , CM000663.1:g.237971964_237971968dup GRCh37
NC_000001.9:g.236038587_236038591dup NCBI36
NG_008799.2:g.771263_771267dup
NG_008799.3:g.771481_771485dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000609119.2:c.*5391-237_*5391-233dup ENSP00000499659.2:n.*5391-237_*5391-233dup
ENST00000659194.3:c.14281-237_14281-233dup ENSP00000499653.3:n.14281-237_14281-233dup
ENST00000660292.2:c.14320-237_14320-233dup ENSP00000499787.2:n.14320-237_14320-233dup
ENST00000659194.2:c.6470-237_6470-233dup
ENST00000366574.7:c.14299-237_14299-233dup MANE Select ENSP00000355533.2:n.14299-237_14299-233dup
ENST00000360064.7:c.14248-237_14248-233dup ENSP00000353174.7:n.14248-237_14248-233dup
ENST00000366574.6:c.14299-237_14299-233dup ENSP00000355533.2:n.14299-237_14299-233dup
ENST00000608590.5:n.810-237_810-233dup
NM_001035.2:c.14299-237_14299-233dup NP_001026.2:n.14299-237_14299-233dup
XM_006711802.2:c.14353-237_14353-233dup XP_006711865.1:n.14353-237_14353-233dup
XM_006711803.2:c.14350-237_14350-233dup XP_006711866.1:n.14350-237_14350-233dup
XM_006711804.2:c.14329-237_14329-233dup XP_006711867.1:n.14329-237_14329-233dup
XM_006711805.2:c.14323-237_14323-233dup XP_006711868.1:n.14323-237_14323-233dup
XM_006711806.2:c.14317-237_14317-233dup XP_006711869.1:n.14317-237_14317-233dup
XM_006711807.2:c.14293-237_14293-233dup XP_006711870.1:n.14293-237_14293-233dup
XM_006711808.2:c.14116-237_14116-233dup XP_006711871.1:n.14116-237_14116-233dup
XM_006711810.2:c.14260-237_14260-233dup XP_006711873.1:n.14260-237_14260-233dup
XM_006711802.3:c.14353-237_14353-233dup XP_006711865.1:n.14353-237_14353-233dup
XM_006711803.3:c.14350-237_14350-233dup XP_006711866.1:n.14350-237_14350-233dup
XM_006711804.3:c.14329-237_14329-233dup XP_006711867.1:n.14329-237_14329-233dup
XM_006711805.3:c.14323-237_14323-233dup XP_006711868.1:n.14323-237_14323-233dup
XM_006711806.3:c.14317-237_14317-233dup XP_006711869.1:n.14317-237_14317-233dup
XM_006711807.3:c.14293-237_14293-233dup XP_006711870.1:n.14293-237_14293-233dup
XM_006711808.3:c.14116-237_14116-233dup XP_006711871.1:n.14116-237_14116-233dup
XM_006711810.3:c.14260-237_14260-233dup XP_006711873.1:n.14260-237_14260-233dup
XM_017002028.1:c.14332-237_14332-233dup XP_016857517.1:n.14332-237_14332-233dup
NM_001035.3:c.14299-237_14299-233dup MANE Select NP_001026.2:n.14299-237_14299-233dup