Canonical Allele Identifier: CA345413324

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947467T>C (hg19) ; chr1:g.237784167T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784167T>C , CM000663.2:g.237784167T>C	GRCh38
NC_000001.10:g.237947467T>C , CM000663.1:g.237947467T>C	GRCh37
NC_000001.9:g.236014090T>C	NCBI36
NG_008799.2:g.746766T>C
NG_008799.3:g.746984T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3547T>C	ENSP00000499659.2:n.*3547T>C
ENST00000659194.3:c.12443T>C	ENSP00000499653.3:p.Ile4148Thr
ENST00000660292.2:c.12476T>C	ENSP00000499787.2:p.Ile4159Thr
ENST00000659194.2:c.4632T>C
ENST00000366574.7:c.12455T>C MANE Select	ENSP00000355533.2:p.Ile4152Thr
ENST00000659194.1:c.4632T>C
ENST00000660292.1:c.2508T>C
ENST00000360064.7:c.12407T>C	ENSP00000353174.7:p.Ile4136Thr
ENST00000366574.6:c.12455T>C	ENSP00000355533.2:p.Ile4152Thr
ENST00000609119.1:n.3650T>C
NM_001035.2:c.12455T>C	NP_001026.2:p.Ile4152Thr
XM_006711802.2:c.12509T>C	XP_006711865.1:p.Ile4170Thr
XM_006711803.2:c.12506T>C	XP_006711866.1:p.Ile4169Thr
XM_006711804.2:c.12485T>C	XP_006711867.1:p.Ile4162Thr
XM_006711805.2:c.12479T>C	XP_006711868.1:p.Ile4160Thr
XM_006711806.2:c.12473T>C	XP_006711869.1:p.Ile4158Thr
XM_006711807.2:c.12449T>C	XP_006711870.1:p.Ile4150Thr
XM_006711808.2:c.12272T>C	XP_006711871.1:p.Ile4091Thr
XM_006711810.2:c.12416T>C	XP_006711873.1:p.Ile4139Thr
XM_006711802.3:c.12509T>C	XP_006711865.1:p.Ile4170Thr
XM_006711803.3:c.12506T>C	XP_006711866.1:p.Ile4169Thr
XM_006711804.3:c.12485T>C	XP_006711867.1:p.Ile4162Thr
XM_006711805.3:c.12479T>C	XP_006711868.1:p.Ile4160Thr
XM_006711806.3:c.12473T>C	XP_006711869.1:p.Ile4158Thr
XM_006711807.3:c.12449T>C	XP_006711870.1:p.Ile4150Thr
XM_006711808.3:c.12272T>C	XP_006711871.1:p.Ile4091Thr
XM_006711810.3:c.12416T>C	XP_006711873.1:p.Ile4139Thr
XM_017002028.1:c.12488T>C	XP_016857517.1:p.Ile4163Thr
NM_001035.3:c.12455T>C MANE Select	NP_001026.2:p.Ile4152Thr