Canonical Allele Identifier: CA345412939

Gene: RYR2

Linked Data

• MyVariant Identifiers: chr1:g.237947323A>C (hg19) ; chr1:g.237784023A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237784023A>C , CM000663.2:g.237784023A>C	GRCh38
NC_000001.10:g.237947323A>C , CM000663.1:g.237947323A>C	GRCh37
NC_000001.9:g.236013946A>C	NCBI36
NG_008799.2:g.746622A>C
NG_008799.3:g.746840A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.*3403A>C	ENSP00000499659.2:n.*3403A>C
ENST00000659194.3:c.12299A>C	ENSP00000499653.3:p.Asn4100Thr
ENST00000660292.2:c.12332A>C	ENSP00000499787.2:p.Asn4111Thr
ENST00000659194.2:c.4488A>C
ENST00000366574.7:c.12311A>C MANE Select	ENSP00000355533.2:p.Asn4104Thr
ENST00000659194.1:c.4488A>C
ENST00000660292.1:c.2364A>C
ENST00000360064.7:c.12263A>C	ENSP00000353174.7:p.Asn4088Thr
ENST00000366574.6:c.12311A>C	ENSP00000355533.2:p.Asn4104Thr
ENST00000609119.1:n.3506A>C
NM_001035.2:c.12311A>C	NP_001026.2:p.Asn4104Thr
XM_006711802.2:c.12365A>C	XP_006711865.1:p.Asn4122Thr
XM_006711803.2:c.12362A>C	XP_006711866.1:p.Asn4121Thr
XM_006711804.2:c.12341A>C	XP_006711867.1:p.Asn4114Thr
XM_006711805.2:c.12335A>C	XP_006711868.1:p.Asn4112Thr
XM_006711806.2:c.12329A>C	XP_006711869.1:p.Asn4110Thr
XM_006711807.2:c.12305A>C	XP_006711870.1:p.Asn4102Thr
XM_006711808.2:c.12128A>C	XP_006711871.1:p.Asn4043Thr
XM_006711810.2:c.12272A>C	XP_006711873.1:p.Asn4091Thr
XM_006711802.3:c.12365A>C	XP_006711865.1:p.Asn4122Thr
XM_006711803.3:c.12362A>C	XP_006711866.1:p.Asn4121Thr
XM_006711804.3:c.12341A>C	XP_006711867.1:p.Asn4114Thr
XM_006711805.3:c.12335A>C	XP_006711868.1:p.Asn4112Thr
XM_006711806.3:c.12329A>C	XP_006711869.1:p.Asn4110Thr
XM_006711807.3:c.12305A>C	XP_006711870.1:p.Asn4102Thr
XM_006711808.3:c.12128A>C	XP_006711871.1:p.Asn4043Thr
XM_006711810.3:c.12272A>C	XP_006711873.1:p.Asn4091Thr
XM_017002028.1:c.12344A>C	XP_016857517.1:p.Asn4115Thr
NM_001035.3:c.12311A>C MANE Select	NP_001026.2:p.Asn4104Thr