Canonical Allele Identifier: CA2487482431
Gene: RYR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237784219A= , CM000663.2:g.237784219A= GRCh38
NC_000001.10:g.237947519A= , CM000663.1:g.237947519A= GRCh37
NC_000001.9:g.236014142A= NCBI36
NG_008799.2:g.746818A=
NG_008799.3:g.747036A=

Transcript Alleles

HGVS Amino-acid change
ENST00000609119.2:c.*3599A= ENSP00000499659.2:n.*3599A=
ENST00000659194.3:c.12495A= ENSP00000499653.3:p.Lys4165=
ENST00000660292.2:c.12528A= ENSP00000499787.2:p.Lys4176=
ENST00000659194.2:c.4684A=
ENST00000366574.7:c.12507A= MANE Select ENSP00000355533.2:p.Lys4169=
ENST00000659194.1:c.4684A=
ENST00000660292.1:c.2560A=
ENST00000360064.7:c.12459A= ENSP00000353174.7:p.Lys4153=
ENST00000366574.6:c.12507A= ENSP00000355533.2:p.Lys4169=
ENST00000609119.1:n.3702A=
NM_001035.2:c.12507A= NP_001026.2:p.Lys4169=
XM_006711802.2:c.12561A= XP_006711865.1:p.Lys4187=
XM_006711803.2:c.12558A= XP_006711866.1:p.Lys4186=
XM_006711804.2:c.12537A= XP_006711867.1:p.Lys4179=
XM_006711805.2:c.12531A= XP_006711868.1:p.Lys4177=
XM_006711806.2:c.12525A= XP_006711869.1:p.Lys4175=
XM_006711807.2:c.12501A= XP_006711870.1:p.Lys4167=
XM_006711808.2:c.12324A= XP_006711871.1:p.Lys4108=
XM_006711810.2:c.12468A= XP_006711873.1:p.Lys4156=
XM_006711802.3:c.12561A= XP_006711865.1:p.Lys4187=
XM_006711803.3:c.12558A= XP_006711866.1:p.Lys4186=
XM_006711804.3:c.12537A= XP_006711867.1:p.Lys4179=
XM_006711805.3:c.12531A= XP_006711868.1:p.Lys4177=
XM_006711806.3:c.12525A= XP_006711869.1:p.Lys4175=
XM_006711807.3:c.12501A= XP_006711870.1:p.Lys4167=
XM_006711808.3:c.12324A= XP_006711871.1:p.Lys4108=
XM_006711810.3:c.12468A= XP_006711873.1:p.Lys4156=
XM_017002028.1:c.12540A= XP_016857517.1:p.Lys4180=
NM_001035.3:c.12507A= MANE Select NP_001026.2:p.Lys4169=