Canonical Allele Identifier: CA345402191

Gene: RYR2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237610770G>C , CM000663.2:g.237610770G>C	GRCh38
NC_000001.10:g.237774070G>C , CM000663.1:g.237774070G>C	GRCh37
NC_000001.9:g.235840693G>C	NCBI36
NG_008799.2:g.573369G>C
NG_008799.3:g.573587G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.4692G>C	ENSP00000499659.2:p.Met1564Ile
ENST00000659194.3:c.4692G>C	ENSP00000499653.3:p.Met1564Ile
ENST00000660292.2:c.4692G>C	ENSP00000499787.2:p.Met1564Ile
ENST00000366574.7:c.4692G>C MANE Select	ENSP00000355533.2:p.Met1564Ile
ENST00000360064.7:c.4644G>C	ENSP00000353174.7:p.Met1548Ile
ENST00000366574.6:c.4692G>C	ENSP00000355533.2:p.Met1564Ile
NM_001035.2:c.4692G>C	NP_001026.2:p.Met1564Ile
XM_006711802.2:c.4722G>C	XP_006711865.1:p.Met1574Ile
XM_006711803.2:c.4719G>C	XP_006711866.1:p.Met1573Ile
XM_006711804.2:c.4722G>C	XP_006711867.1:p.Met1574Ile
XM_006711805.2:c.4692G>C	XP_006711868.1:p.Met1564Ile
XM_006711806.2:c.4722G>C	XP_006711869.1:p.Met1574Ile
XM_006711807.2:c.4722G>C	XP_006711870.1:p.Met1574Ile
XM_006711808.2:c.4722G>C	XP_006711871.1:p.Met1574Ile
XM_006711809.2:c.4722G>C	XP_006711872.1:p.Met1574Ile
XM_006711810.2:c.4689G>C	XP_006711873.1:p.Met1563Ile
XR_949152.1:n.5003G>C
XM_006711802.3:c.4722G>C	XP_006711865.1:p.Met1574Ile
XM_006711803.3:c.4719G>C	XP_006711866.1:p.Met1573Ile
XM_006711804.3:c.4722G>C	XP_006711867.1:p.Met1574Ile
XM_006711805.3:c.4692G>C	XP_006711868.1:p.Met1564Ile
XM_006711806.3:c.4722G>C	XP_006711869.1:p.Met1574Ile
XM_006711807.3:c.4722G>C	XP_006711870.1:p.Met1574Ile
XM_006711808.3:c.4722G>C	XP_006711871.1:p.Met1574Ile
XM_006711810.3:c.4689G>C	XP_006711873.1:p.Met1563Ile
XM_017002028.1:c.4701G>C	XP_016857517.1:p.Met1567Ile
XR_002957299.1:n.5036G>C
XR_949152.2:n.5036G>C
NM_001035.3:c.4692G>C MANE Select	NP_001026.2:p.Met1564Ile