Canonical Allele Identifier: CA424032308

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947555A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784255A>G , CM000663.2:g.237784255A>G	GRCh38
NC_000001.10:g.237947555A>G , CM000663.1:g.237947555A>G	GRCh37
NC_000001.9:g.236014178A>G	NCBI36
NG_008799.2:g.746854A>G
NG_008799.3:g.747072A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3635A>G	ENSP00000499659.2:n.*3635A>G
ENST00000659194.3:c.12531A>G	ENSP00000499653.3:p.Gly4177=
ENST00000660292.2:c.12564A>G	ENSP00000499787.2:p.Gly4188=
ENST00000659194.2:c.4720A>G
ENST00000366574.7:c.12543A>G MANE Select	ENSP00000355533.2:p.Gly4181=
ENST00000659194.1:c.4720A>G
ENST00000660292.1:c.2596A>G
ENST00000360064.7:c.12495A>G	ENSP00000353174.7:p.Gly4165=
ENST00000366574.6:c.12543A>G	ENSP00000355533.2:p.Gly4181=
ENST00000609119.1:n.3738A>G
NM_001035.2:c.12543A>G	NP_001026.2:p.Gly4181=
XM_006711802.2:c.12597A>G	XP_006711865.1:p.Gly4199=
XM_006711803.2:c.12594A>G	XP_006711866.1:p.Gly4198=
XM_006711804.2:c.12573A>G	XP_006711867.1:p.Gly4191=
XM_006711805.2:c.12567A>G	XP_006711868.1:p.Gly4189=
XM_006711806.2:c.12561A>G	XP_006711869.1:p.Gly4187=
XM_006711807.2:c.12537A>G	XP_006711870.1:p.Gly4179=
XM_006711808.2:c.12360A>G	XP_006711871.1:p.Gly4120=
XM_006711810.2:c.12504A>G	XP_006711873.1:p.Gly4168=
XM_006711802.3:c.12597A>G	XP_006711865.1:p.Gly4199=
XM_006711803.3:c.12594A>G	XP_006711866.1:p.Gly4198=
XM_006711804.3:c.12573A>G	XP_006711867.1:p.Gly4191=
XM_006711805.3:c.12567A>G	XP_006711868.1:p.Gly4189=
XM_006711806.3:c.12561A>G	XP_006711869.1:p.Gly4187=
XM_006711807.3:c.12537A>G	XP_006711870.1:p.Gly4179=
XM_006711808.3:c.12360A>G	XP_006711871.1:p.Gly4120=
XM_006711810.3:c.12504A>G	XP_006711873.1:p.Gly4168=
XM_017002028.1:c.12576A>G	XP_016857517.1:p.Gly4192=
NM_001035.3:c.12543A>G MANE Select	NP_001026.2:p.Gly4181=