Canonical Allele Identifier: CA345413576

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947550G>A (hg19) ; chr1:g.237784250G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784250G>A , CM000663.2:g.237784250G>A	GRCh38
NC_000001.10:g.237947550G>A , CM000663.1:g.237947550G>A	GRCh37
NC_000001.9:g.236014173G>A	NCBI36
NG_008799.2:g.746849G>A
NG_008799.3:g.747067G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3630G>A	ENSP00000499659.2:n.*3630G>A
ENST00000659194.3:c.12526G>A	ENSP00000499653.3:p.Gly4176Ser
ENST00000660292.2:c.12559G>A	ENSP00000499787.2:p.Gly4187Ser
ENST00000659194.2:c.4715G>A
ENST00000366574.7:c.12538G>A MANE Select	ENSP00000355533.2:p.Gly4180Ser
ENST00000659194.1:c.4715G>A
ENST00000660292.1:c.2591G>A
ENST00000360064.7:c.12490G>A	ENSP00000353174.7:p.Gly4164Ser
ENST00000366574.6:c.12538G>A	ENSP00000355533.2:p.Gly4180Ser
ENST00000609119.1:n.3733G>A
NM_001035.2:c.12538G>A	NP_001026.2:p.Gly4180Ser
XM_006711802.2:c.12592G>A	XP_006711865.1:p.Gly4198Ser
XM_006711803.2:c.12589G>A	XP_006711866.1:p.Gly4197Ser
XM_006711804.2:c.12568G>A	XP_006711867.1:p.Gly4190Ser
XM_006711805.2:c.12562G>A	XP_006711868.1:p.Gly4188Ser
XM_006711806.2:c.12556G>A	XP_006711869.1:p.Gly4186Ser
XM_006711807.2:c.12532G>A	XP_006711870.1:p.Gly4178Ser
XM_006711808.2:c.12355G>A	XP_006711871.1:p.Gly4119Ser
XM_006711810.2:c.12499G>A	XP_006711873.1:p.Gly4167Ser
XM_006711802.3:c.12592G>A	XP_006711865.1:p.Gly4198Ser
XM_006711803.3:c.12589G>A	XP_006711866.1:p.Gly4197Ser
XM_006711804.3:c.12568G>A	XP_006711867.1:p.Gly4190Ser
XM_006711805.3:c.12562G>A	XP_006711868.1:p.Gly4188Ser
XM_006711806.3:c.12556G>A	XP_006711869.1:p.Gly4186Ser
XM_006711807.3:c.12532G>A	XP_006711870.1:p.Gly4178Ser
XM_006711808.3:c.12355G>A	XP_006711871.1:p.Gly4119Ser
XM_006711810.3:c.12499G>A	XP_006711873.1:p.Gly4167Ser
XM_017002028.1:c.12571G>A	XP_016857517.1:p.Gly4191Ser
NM_001035.3:c.12538G>A MANE Select	NP_001026.2:p.Gly4180Ser