Canonical Allele Identifier: CA345413280

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947455T>G (hg19) ; chr1:g.237784155T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784155T>G , CM000663.2:g.237784155T>G	GRCh38
NC_000001.10:g.237947455T>G , CM000663.1:g.237947455T>G	GRCh37
NC_000001.9:g.236014078T>G	NCBI36
NG_008799.2:g.746754T>G
NG_008799.3:g.746972T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3535T>G	ENSP00000499659.2:n.*3535T>G
ENST00000659194.3:c.12431T>G	ENSP00000499653.3:p.Val4144Gly
ENST00000660292.2:c.12464T>G	ENSP00000499787.2:p.Val4155Gly
ENST00000659194.2:c.4620T>G
ENST00000366574.7:c.12443T>G MANE Select	ENSP00000355533.2:p.Val4148Gly
ENST00000659194.1:c.4620T>G
ENST00000660292.1:c.2496T>G
ENST00000360064.7:c.12395T>G	ENSP00000353174.7:p.Val4132Gly
ENST00000366574.6:c.12443T>G	ENSP00000355533.2:p.Val4148Gly
ENST00000609119.1:n.3638T>G
NM_001035.2:c.12443T>G	NP_001026.2:p.Val4148Gly
XM_006711802.2:c.12497T>G	XP_006711865.1:p.Val4166Gly
XM_006711803.2:c.12494T>G	XP_006711866.1:p.Val4165Gly
XM_006711804.2:c.12473T>G	XP_006711867.1:p.Val4158Gly
XM_006711805.2:c.12467T>G	XP_006711868.1:p.Val4156Gly
XM_006711806.2:c.12461T>G	XP_006711869.1:p.Val4154Gly
XM_006711807.2:c.12437T>G	XP_006711870.1:p.Val4146Gly
XM_006711808.2:c.12260T>G	XP_006711871.1:p.Val4087Gly
XM_006711810.2:c.12404T>G	XP_006711873.1:p.Val4135Gly
XM_006711802.3:c.12497T>G	XP_006711865.1:p.Val4166Gly
XM_006711803.3:c.12494T>G	XP_006711866.1:p.Val4165Gly
XM_006711804.3:c.12473T>G	XP_006711867.1:p.Val4158Gly
XM_006711805.3:c.12467T>G	XP_006711868.1:p.Val4156Gly
XM_006711806.3:c.12461T>G	XP_006711869.1:p.Val4154Gly
XM_006711807.3:c.12437T>G	XP_006711870.1:p.Val4146Gly
XM_006711808.3:c.12260T>G	XP_006711871.1:p.Val4087Gly
XM_006711810.3:c.12404T>G	XP_006711873.1:p.Val4135Gly
XM_017002028.1:c.12476T>G	XP_016857517.1:p.Val4159Gly
NM_001035.3:c.12443T>G MANE Select	NP_001026.2:p.Val4148Gly