Canonical Allele Identifier: CA345424489

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237972311T>G (hg19) ; chr1:g.237809011T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237809011T>G , CM000663.2:g.237809011T>G	GRCh38
NC_000001.10:g.237972311T>G , CM000663.1:g.237972311T>G	GRCh37
NC_000001.9:g.236038934T>G	NCBI36
NG_008799.2:g.771610T>G
NG_008799.3:g.771828T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5501T>G	ENSP00000499659.2:n.*5501T>G
ENST00000659194.3:c.14391T>G	ENSP00000499653.3:p.Asp4797Glu
ENST00000660292.2:c.14430T>G	ENSP00000499787.2:p.Asp4810Glu
ENST00000659194.2:c.6580T>G
ENST00000366574.7:c.14409T>G MANE Select	ENSP00000355533.2:p.Asp4803Glu
ENST00000360064.7:c.14358T>G	ENSP00000353174.7:p.Asp4786Glu
ENST00000366574.6:c.14409T>G	ENSP00000355533.2:p.Asp4803Glu
ENST00000608590.5:n.920T>G
NM_001035.2:c.14409T>G	NP_001026.2:p.Asp4803Glu
XM_006711802.2:c.14463T>G	XP_006711865.1:p.Asp4821Glu
XM_006711803.2:c.14460T>G	XP_006711866.1:p.Asp4820Glu
XM_006711804.2:c.14439T>G	XP_006711867.1:p.Asp4813Glu
XM_006711805.2:c.14433T>G	XP_006711868.1:p.Asp4811Glu
XM_006711806.2:c.14427T>G	XP_006711869.1:p.Asp4809Glu
XM_006711807.2:c.14403T>G	XP_006711870.1:p.Asp4801Glu
XM_006711808.2:c.14226T>G	XP_006711871.1:p.Asp4742Glu
XM_006711810.2:c.14370T>G	XP_006711873.1:p.Asp4790Glu
XM_006711802.3:c.14463T>G	XP_006711865.1:p.Asp4821Glu
XM_006711803.3:c.14460T>G	XP_006711866.1:p.Asp4820Glu
XM_006711804.3:c.14439T>G	XP_006711867.1:p.Asp4813Glu
XM_006711805.3:c.14433T>G	XP_006711868.1:p.Asp4811Glu
XM_006711806.3:c.14427T>G	XP_006711869.1:p.Asp4809Glu
XM_006711807.3:c.14403T>G	XP_006711870.1:p.Asp4801Glu
XM_006711808.3:c.14226T>G	XP_006711871.1:p.Asp4742Glu
XM_006711810.3:c.14370T>G	XP_006711873.1:p.Asp4790Glu
XM_017002028.1:c.14442T>G	XP_016857517.1:p.Asp4814Glu
NM_001035.3:c.14409T>G MANE Select	NP_001026.2:p.Asp4803Glu