Canonical Allele Identifier: CA087611
Community Standard Title: NM_001035.3(RYR2):c.8314C>T (p.Arg2772Cys)
Gene: RYR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237660825C>T , CM000663.2:g.237660825C>T GRCh38
NC_000001.10:g.237824125C>T , CM000663.1:g.237824125C>T GRCh37
NC_000001.9:g.235890748C>T NCBI36
NG_008799.2:g.623424C>T
NG_008799.3:g.623642C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001035.3:c.8314C>T MANE Select NP_001026.2:p.Arg2772Cys
ENST00000366574.7:c.8314C>T MANE Select ENSP00000355533.2:p.Arg2772Cys
NM_001035.2:c.8314C>T NP_001026.2:p.Arg2772Cys
ENST00000360064.7:c.8266C>T ENSP00000353174.7:p.Arg2756Cys
ENST00000366574.6:c.8314C>T ENSP00000355533.2:p.Arg2772Cys
ENST00000609119.2:c.8314C>T ENSP00000499659.2:p.Arg2772Cys
ENST00000659194.1:c.503C>T
ENST00000659194.2:c.503C>T
ENST00000659194.3:c.8314C>T ENSP00000499653.3:p.Arg2772Cys
ENST00000660292.2:c.8314C>T ENSP00000499787.2:p.Arg2772Cys
XM_006711802.2:c.8344C>T XP_006711865.1:p.Arg2782Cys
XM_006711802.3:c.8344C>T XP_006711865.1:p.Arg2782Cys
XM_006711803.2:c.8341C>T XP_006711866.1:p.Arg2781Cys
XM_006711803.3:c.8341C>T XP_006711866.1:p.Arg2781Cys
XM_006711804.2:c.8344C>T XP_006711867.1:p.Arg2782Cys
XM_006711804.3:c.8344C>T XP_006711867.1:p.Arg2782Cys
XM_006711805.2:c.8314C>T XP_006711868.1:p.Arg2772Cys
XM_006711805.3:c.8314C>T XP_006711868.1:p.Arg2772Cys
XM_006711806.2:c.8344C>T XP_006711869.1:p.Arg2782Cys
XM_006711806.3:c.8344C>T XP_006711869.1:p.Arg2782Cys
XM_006711807.2:c.8344C>T XP_006711870.1:p.Arg2782Cys
XM_006711807.3:c.8344C>T XP_006711870.1:p.Arg2782Cys
XM_006711808.2:c.8344C>T XP_006711871.1:p.Arg2782Cys
XM_006711808.3:c.8344C>T XP_006711871.1:p.Arg2782Cys
XM_006711810.2:c.8311C>T XP_006711873.1:p.Arg2771Cys
XM_006711810.3:c.8311C>T XP_006711873.1:p.Arg2771Cys
XM_017002028.1:c.8323C>T XP_016857517.1:p.Arg2775Cys
XR_002957299.1:n.8725C>T
XR_949152.1:n.8625C>T
XR_949152.2:n.8658C>T