Canonical Allele Identifier: CA345412898

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947302A>T (hg19) ; chr1:g.237784002A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784002A>T , CM000663.2:g.237784002A>T	GRCh38
NC_000001.10:g.237947302A>T , CM000663.1:g.237947302A>T	GRCh37
NC_000001.9:g.236013925A>T	NCBI36
NG_008799.2:g.746601A>T
NG_008799.3:g.746819A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3382A>T	ENSP00000499659.2:n.*3382A>T
ENST00000659194.3:c.12278A>T	ENSP00000499653.3:p.Asn4093Ile
ENST00000660292.2:c.12311A>T	ENSP00000499787.2:p.Asn4104Ile
ENST00000659194.2:c.4467A>T
ENST00000366574.7:c.12290A>T MANE Select	ENSP00000355533.2:p.Asn4097Ile
ENST00000659194.1:c.4467A>T
ENST00000660292.1:c.2343A>T
ENST00000360064.7:c.12242A>T	ENSP00000353174.7:p.Asn4081Ile
ENST00000366574.6:c.12290A>T	ENSP00000355533.2:p.Asn4097Ile
ENST00000609119.1:n.3485A>T
NM_001035.2:c.12290A>T	NP_001026.2:p.Asn4097Ile
XM_006711802.2:c.12344A>T	XP_006711865.1:p.Asn4115Ile
XM_006711803.2:c.12341A>T	XP_006711866.1:p.Asn4114Ile
XM_006711804.2:c.12320A>T	XP_006711867.1:p.Asn4107Ile
XM_006711805.2:c.12314A>T	XP_006711868.1:p.Asn4105Ile
XM_006711806.2:c.12308A>T	XP_006711869.1:p.Asn4103Ile
XM_006711807.2:c.12284A>T	XP_006711870.1:p.Asn4095Ile
XM_006711808.2:c.12107A>T	XP_006711871.1:p.Asn4036Ile
XM_006711810.2:c.12251A>T	XP_006711873.1:p.Asn4084Ile
XM_006711802.3:c.12344A>T	XP_006711865.1:p.Asn4115Ile
XM_006711803.3:c.12341A>T	XP_006711866.1:p.Asn4114Ile
XM_006711804.3:c.12320A>T	XP_006711867.1:p.Asn4107Ile
XM_006711805.3:c.12314A>T	XP_006711868.1:p.Asn4105Ile
XM_006711806.3:c.12308A>T	XP_006711869.1:p.Asn4103Ile
XM_006711807.3:c.12284A>T	XP_006711870.1:p.Asn4095Ile
XM_006711808.3:c.12107A>T	XP_006711871.1:p.Asn4036Ile
XM_006711810.3:c.12251A>T	XP_006711873.1:p.Asn4084Ile
XM_017002028.1:c.12323A>T	XP_016857517.1:p.Asn4108Ile
NM_001035.3:c.12290A>T MANE Select	NP_001026.2:p.Asn4097Ile