Canonical Allele Identifier: CA345403695

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237841396T>G (hg19) ; chr1:g.237678096T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237678096T>G , CM000663.2:g.237678096T>G	GRCh38
NC_000001.10:g.237841396T>G , CM000663.1:g.237841396T>G	GRCh37
NC_000001.9:g.235908019T>G	NCBI36
NG_008799.2:g.640695T>G
NG_008799.3:g.640913T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.8831-2360T>G	ENSP00000499659.2:n.8831-2360T>G
ENST00000659194.3:c.8879T>G	ENSP00000499653.3:p.Ile2960Ser
ENST00000660292.2:c.8879T>G	ENSP00000499787.2:p.Ile2960Ser
ENST00000659194.2:c.1068T>G
ENST00000366574.7:c.8879T>G MANE Select	ENSP00000355533.2:p.Ile2960Ser
ENST00000659194.1:c.1068T>G
ENST00000360064.7:c.8831T>G	ENSP00000353174.7:p.Ile2944Ser
ENST00000366574.6:c.8879T>G	ENSP00000355533.2:p.Ile2960Ser
ENST00000609119.1:n.84-2360T>G
NM_001035.2:c.8879T>G	NP_001026.2:p.Ile2960Ser
XM_006711802.2:c.8909T>G	XP_006711865.1:p.Ile2970Ser
XM_006711803.2:c.8906T>G	XP_006711866.1:p.Ile2969Ser
XM_006711804.2:c.8909T>G	XP_006711867.1:p.Ile2970Ser
XM_006711805.2:c.8879T>G	XP_006711868.1:p.Ile2960Ser
XM_006711806.2:c.8909T>G	XP_006711869.1:p.Ile2970Ser
XM_006711807.2:c.8909T>G	XP_006711870.1:p.Ile2970Ser
XM_006711808.2:c.8860+3250T>G	XP_006711871.1:n.8860+3250T>G
XM_006711810.2:c.8876T>G	XP_006711873.1:p.Ile2959Ser
XR_949152.1:n.9190T>G
XM_006711802.3:c.8909T>G	XP_006711865.1:p.Ile2970Ser
XM_006711803.3:c.8906T>G	XP_006711866.1:p.Ile2969Ser
XM_006711804.3:c.8909T>G	XP_006711867.1:p.Ile2970Ser
XM_006711805.3:c.8879T>G	XP_006711868.1:p.Ile2960Ser
XM_006711806.3:c.8909T>G	XP_006711869.1:p.Ile2970Ser
XM_006711807.3:c.8909T>G	XP_006711870.1:p.Ile2970Ser
XM_006711808.3:c.8860+3250T>G	XP_006711871.1:n.8860+3250T>G
XM_006711810.3:c.8876T>G	XP_006711873.1:p.Ile2959Ser
XM_017002028.1:c.8888T>G	XP_016857517.1:p.Ile2963Ser
XR_949152.2:n.9223T>G
NM_001035.3:c.8879T>G MANE Select	NP_001026.2:p.Ile2960Ser