Canonical Allele Identifier: CA423818848

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237701994G>A , CM000663.2:g.237701994G>A	GRCh38
NC_000001.10:g.237865294G>A , CM000663.1:g.237865294G>A	GRCh37
NC_000001.9:g.235931917G>A	NCBI36
NG_008799.2:g.664593G>A
NG_008799.3:g.664811G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.9384G>A MANE Select	NP_001026.2:p.Val3128=
ENST00000366574.7:c.9384G>A MANE Select	ENSP00000355533.2:p.Val3128=
NM_001035.2:c.9384G>A	NP_001026.2:p.Val3128=
ENST00000360064.7:c.9336G>A	ENSP00000353174.7:p.Val3112=
ENST00000366574.6:c.9384G>A	ENSP00000355533.2:p.Val3128=
ENST00000609119.1:n.522G>A
ENST00000609119.2:c.*419G>A	ENSP00000499659.2:n.*419G>A
ENST00000659194.1:c.1573G>A
ENST00000659194.2:c.1573G>A
ENST00000659194.3:c.9384G>A	ENSP00000499653.3:p.Val3128=
ENST00000660292.2:c.9384G>A	ENSP00000499787.2:p.Val3128=
XM_006711802.2:c.9414G>A	XP_006711865.1:p.Val3138=
XM_006711802.3:c.9414G>A	XP_006711865.1:p.Val3138=
XM_006711803.2:c.9411G>A	XP_006711866.1:p.Val3137=
XM_006711803.3:c.9411G>A	XP_006711866.1:p.Val3137=
XM_006711804.2:c.9414G>A	XP_006711867.1:p.Val3138=
XM_006711804.3:c.9414G>A	XP_006711867.1:p.Val3138=
XM_006711805.2:c.9384G>A	XP_006711868.1:p.Val3128=
XM_006711805.3:c.9384G>A	XP_006711868.1:p.Val3128=
XM_006711806.2:c.9414G>A	XP_006711869.1:p.Val3138=
XM_006711806.3:c.9414G>A	XP_006711869.1:p.Val3138=
XM_006711807.2:c.9414G>A	XP_006711870.1:p.Val3138=
XM_006711807.3:c.9414G>A	XP_006711870.1:p.Val3138=
XM_006711808.2:c.9177G>A	XP_006711871.1:p.Val3059=
XM_006711808.3:c.9177G>A	XP_006711871.1:p.Val3059=
XM_006711810.2:c.9381G>A	XP_006711873.1:p.Val3127=
XM_006711810.3:c.9381G>A	XP_006711873.1:p.Val3127=
XM_017002028.1:c.9393G>A	XP_016857517.1:p.Val3131=
XR_949152.1:n.9645G>A
XR_949152.2:n.9678G>A