Canonical Allele Identifier: CA345424337

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237972278C>G (hg19) ; chr1:g.237808978C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237808978C>G , CM000663.2:g.237808978C>G	GRCh38
NC_000001.10:g.237972278C>G , CM000663.1:g.237972278C>G	GRCh37
NC_000001.9:g.236038901C>G	NCBI36
NG_008799.2:g.771577C>G
NG_008799.3:g.771795C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*5468C>G	ENSP00000499659.2:n.*5468C>G
ENST00000659194.3:c.14358C>G	ENSP00000499653.3:p.Phe4786Leu
ENST00000660292.2:c.14397C>G	ENSP00000499787.2:p.Phe4799Leu
ENST00000659194.2:c.6547C>G
ENST00000366574.7:c.14376C>G MANE Select	ENSP00000355533.2:p.Phe4792Leu
ENST00000360064.7:c.14325C>G	ENSP00000353174.7:p.Phe4775Leu
ENST00000366574.6:c.14376C>G	ENSP00000355533.2:p.Phe4792Leu
ENST00000608590.5:n.887C>G
NM_001035.2:c.14376C>G	NP_001026.2:p.Phe4792Leu
XM_006711802.2:c.14430C>G	XP_006711865.1:p.Phe4810Leu
XM_006711803.2:c.14427C>G	XP_006711866.1:p.Phe4809Leu
XM_006711804.2:c.14406C>G	XP_006711867.1:p.Phe4802Leu
XM_006711805.2:c.14400C>G	XP_006711868.1:p.Phe4800Leu
XM_006711806.2:c.14394C>G	XP_006711869.1:p.Phe4798Leu
XM_006711807.2:c.14370C>G	XP_006711870.1:p.Phe4790Leu
XM_006711808.2:c.14193C>G	XP_006711871.1:p.Phe4731Leu
XM_006711810.2:c.14337C>G	XP_006711873.1:p.Phe4779Leu
XM_006711802.3:c.14430C>G	XP_006711865.1:p.Phe4810Leu
XM_006711803.3:c.14427C>G	XP_006711866.1:p.Phe4809Leu
XM_006711804.3:c.14406C>G	XP_006711867.1:p.Phe4802Leu
XM_006711805.3:c.14400C>G	XP_006711868.1:p.Phe4800Leu
XM_006711806.3:c.14394C>G	XP_006711869.1:p.Phe4798Leu
XM_006711807.3:c.14370C>G	XP_006711870.1:p.Phe4790Leu
XM_006711808.3:c.14193C>G	XP_006711871.1:p.Phe4731Leu
XM_006711810.3:c.14337C>G	XP_006711873.1:p.Phe4779Leu
XM_017002028.1:c.14409C>G	XP_016857517.1:p.Phe4803Leu
NM_001035.3:c.14376C>G MANE Select	NP_001026.2:p.Phe4792Leu