Canonical Allele Identifier: CA345413520

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947527T>A (hg19) ; chr1:g.237784227T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784227T>A , CM000663.2:g.237784227T>A	GRCh38
NC_000001.10:g.237947527T>A , CM000663.1:g.237947527T>A	GRCh37
NC_000001.9:g.236014150T>A	NCBI36
NG_008799.2:g.746826T>A
NG_008799.3:g.747044T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000609119.2:c.*3607T>A	ENSP00000499659.2:n.*3607T>A
ENST00000659194.3:c.12503T>A	ENSP00000499653.3:p.Phe4168Tyr
ENST00000660292.2:c.12536T>A	ENSP00000499787.2:p.Phe4179Tyr
ENST00000659194.2:c.4692T>A
ENST00000366574.7:c.12515T>A MANE Select	ENSP00000355533.2:p.Phe4172Tyr
ENST00000659194.1:c.4692T>A
ENST00000660292.1:c.2568T>A
ENST00000360064.7:c.12467T>A	ENSP00000353174.7:p.Phe4156Tyr
ENST00000366574.6:c.12515T>A	ENSP00000355533.2:p.Phe4172Tyr
ENST00000609119.1:n.3710T>A
NM_001035.2:c.12515T>A	NP_001026.2:p.Phe4172Tyr
XM_006711802.2:c.12569T>A	XP_006711865.1:p.Phe4190Tyr
XM_006711803.2:c.12566T>A	XP_006711866.1:p.Phe4189Tyr
XM_006711804.2:c.12545T>A	XP_006711867.1:p.Phe4182Tyr
XM_006711805.2:c.12539T>A	XP_006711868.1:p.Phe4180Tyr
XM_006711806.2:c.12533T>A	XP_006711869.1:p.Phe4178Tyr
XM_006711807.2:c.12509T>A	XP_006711870.1:p.Phe4170Tyr
XM_006711808.2:c.12332T>A	XP_006711871.1:p.Phe4111Tyr
XM_006711810.2:c.12476T>A	XP_006711873.1:p.Phe4159Tyr
XM_006711802.3:c.12569T>A	XP_006711865.1:p.Phe4190Tyr
XM_006711803.3:c.12566T>A	XP_006711866.1:p.Phe4189Tyr
XM_006711804.3:c.12545T>A	XP_006711867.1:p.Phe4182Tyr
XM_006711805.3:c.12539T>A	XP_006711868.1:p.Phe4180Tyr
XM_006711806.3:c.12533T>A	XP_006711869.1:p.Phe4178Tyr
XM_006711807.3:c.12509T>A	XP_006711870.1:p.Phe4170Tyr
XM_006711808.3:c.12332T>A	XP_006711871.1:p.Phe4111Tyr
XM_006711810.3:c.12476T>A	XP_006711873.1:p.Phe4159Tyr
XM_017002028.1:c.12548T>A	XP_016857517.1:p.Phe4183Tyr
NM_001035.3:c.12515T>A MANE Select	NP_001026.2:p.Phe4172Tyr