Canonical Allele Identifier: CA009911

Gene: RYR2

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237614747A>G , CM000663.2:g.237614747A>G	GRCh38
NC_000001.10:g.237778047A>G , CM000663.1:g.237778047A>G	GRCh37
NC_000001.9:g.235844670A>G	NCBI36
NG_008799.2:g.577346A>G
NG_008799.3:g.577564A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.5619A>G	ENSP00000499659.2:p.Ala1873=
ENST00000659194.3:c.5619A>G	ENSP00000499653.3:p.Ala1873=
ENST00000660292.2:c.5619A>G	ENSP00000499787.2:p.Ala1873=
ENST00000366574.7:c.5619A>G MANE Select	ENSP00000355533.2:p.Ala1873=
ENST00000360064.7:c.5571A>G	ENSP00000353174.7:p.Ala1857=
ENST00000366574.6:c.5619A>G	ENSP00000355533.2:p.Ala1873=
NM_001035.2:c.5619A>G	NP_001026.2:p.Ala1873=
XM_006711802.2:c.5649A>G	XP_006711865.1:p.Ala1883=
XM_006711803.2:c.5646A>G	XP_006711866.1:p.Ala1882=
XM_006711804.2:c.5649A>G	XP_006711867.1:p.Ala1883=
XM_006711805.2:c.5619A>G	XP_006711868.1:p.Ala1873=
XM_006711806.2:c.5649A>G	XP_006711869.1:p.Ala1883=
XM_006711807.2:c.5649A>G	XP_006711870.1:p.Ala1883=
XM_006711808.2:c.5649A>G	XP_006711871.1:p.Ala1883=
XM_006711809.2:c.5649A>G	XP_006711872.1:p.Ala1883=
XM_006711810.2:c.5616A>G	XP_006711873.1:p.Ala1872=
XR_949152.1:n.5930A>G
XM_006711802.3:c.5649A>G	XP_006711865.1:p.Ala1883=
XM_006711803.3:c.5646A>G	XP_006711866.1:p.Ala1882=
XM_006711804.3:c.5649A>G	XP_006711867.1:p.Ala1883=
XM_006711805.3:c.5619A>G	XP_006711868.1:p.Ala1873=
XM_006711806.3:c.5649A>G	XP_006711869.1:p.Ala1883=
XM_006711807.3:c.5649A>G	XP_006711870.1:p.Ala1883=
XM_006711808.3:c.5649A>G	XP_006711871.1:p.Ala1883=
XM_006711810.3:c.5616A>G	XP_006711873.1:p.Ala1872=
XM_017002028.1:c.5628A>G	XP_016857517.1:p.Ala1876=
XR_002957299.1:n.5963A>G
XR_949152.2:n.5963A>G
NM_001035.3:c.5619A>G MANE Select	NP_001026.2:p.Ala1873=