Canonical Allele Identifier: CA345408307

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237706967A>C , CM000663.2:g.237706967A>C	GRCh38
NC_000001.10:g.237870267A>C , CM000663.1:g.237870267A>C	GRCh37
NC_000001.9:g.235936890A>C	NCBI36
NG_008799.2:g.669566A>C
NG_008799.3:g.669784A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001035.3:c.9599A>C MANE Select	NP_001026.2:p.Asn3200Thr
ENST00000366574.7:c.9599A>C MANE Select	ENSP00000355533.2:p.Asn3200Thr
NM_001035.2:c.9599A>C	NP_001026.2:p.Asn3200Thr
ENST00000360064.7:c.9551A>C	ENSP00000353174.7:p.Asn3184Thr
ENST00000366574.6:c.9599A>C	ENSP00000355533.2:p.Asn3200Thr
ENST00000609119.1:n.737A>C
ENST00000609119.2:c.*634A>C	ENSP00000499659.2:n.*634A>C
ENST00000659194.1:c.1788A>C
ENST00000659194.2:c.1788A>C
ENST00000659194.3:c.9599A>C	ENSP00000499653.3:p.Asn3200Thr
ENST00000660292.2:c.9599A>C	ENSP00000499787.2:p.Asn3200Thr
XM_006711802.2:c.9629A>C	XP_006711865.1:p.Asn3210Thr
XM_006711802.3:c.9629A>C	XP_006711865.1:p.Asn3210Thr
XM_006711803.2:c.9626A>C	XP_006711866.1:p.Asn3209Thr
XM_006711803.3:c.9626A>C	XP_006711866.1:p.Asn3209Thr
XM_006711804.2:c.9629A>C	XP_006711867.1:p.Asn3210Thr
XM_006711804.3:c.9629A>C	XP_006711867.1:p.Asn3210Thr
XM_006711805.2:c.9599A>C	XP_006711868.1:p.Asn3200Thr
XM_006711805.3:c.9599A>C	XP_006711868.1:p.Asn3200Thr
XM_006711806.2:c.9629A>C	XP_006711869.1:p.Asn3210Thr
XM_006711806.3:c.9629A>C	XP_006711869.1:p.Asn3210Thr
XM_006711807.2:c.9629A>C	XP_006711870.1:p.Asn3210Thr
XM_006711807.3:c.9629A>C	XP_006711870.1:p.Asn3210Thr
XM_006711808.2:c.9392A>C	XP_006711871.1:p.Asn3131Thr
XM_006711808.3:c.9392A>C	XP_006711871.1:p.Asn3131Thr
XM_006711810.2:c.9596A>C	XP_006711873.1:p.Asn3199Thr
XM_006711810.3:c.9596A>C	XP_006711873.1:p.Asn3199Thr
XM_017002028.1:c.9608A>C	XP_016857517.1:p.Asn3203Thr