Canonical Allele Identifier: CA2487426800
Gene: RYR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.237648389A= , CM000663.2:g.237648389A= GRCh38
NC_000001.10:g.237811689A= , CM000663.1:g.237811689A= GRCh37
NC_000001.9:g.235878312A= NCBI36
NG_008799.2:g.610988A=
NG_008799.3:g.611206A=

Transcript Alleles

HGVS Amino-acid change
ENST00000609119.2:c.7343-55A= ENSP00000499659.2:n.7343-55A=
ENST00000659194.3:c.7343-55A= ENSP00000499653.3:n.7343-55A=
ENST00000660292.2:c.7343-55A= ENSP00000499787.2:n.7343-55A=
ENST00000366574.7:c.7343-55A= MANE Select ENSP00000355533.2:n.7343-55A=
ENST00000360064.7:c.7295-55A= ENSP00000353174.7:n.7295-55A=
ENST00000366574.6:c.7343-55A= ENSP00000355533.2:n.7343-55A=
NM_001035.2:c.7343-55A= NP_001026.2:n.7343-55A=
XM_006711802.2:c.7373-55A= XP_006711865.1:n.7373-55A=
XM_006711803.2:c.7370-55A= XP_006711866.1:n.7370-55A=
XM_006711804.2:c.7373-55A= XP_006711867.1:n.7373-55A=
XM_006711805.2:c.7343-55A= XP_006711868.1:n.7343-55A=
XM_006711806.2:c.7373-55A= XP_006711869.1:n.7373-55A=
XM_006711807.2:c.7373-55A= XP_006711870.1:n.7373-55A=
XM_006711808.2:c.7373-55A= XP_006711871.1:n.7373-55A=
XM_006711809.2:c.7373-55A= XP_006711872.1:n.7373-55A=
XM_006711810.2:c.7340-55A= XP_006711873.1:n.7340-55A=
XR_949152.1:n.7654-55A=
XM_006711802.3:c.7373-55A= XP_006711865.1:n.7373-55A=
XM_006711803.3:c.7370-55A= XP_006711866.1:n.7370-55A=
XM_006711804.3:c.7373-55A= XP_006711867.1:n.7373-55A=
XM_006711805.3:c.7343-55A= XP_006711868.1:n.7343-55A=
XM_006711806.3:c.7373-55A= XP_006711869.1:n.7373-55A=
XM_006711807.3:c.7373-55A= XP_006711870.1:n.7373-55A=
XM_006711808.3:c.7373-55A= XP_006711871.1:n.7373-55A=
XM_006711810.3:c.7340-55A= XP_006711873.1:n.7340-55A=
XM_017002028.1:c.7352-55A= XP_016857517.1:n.7352-55A=
XR_002957299.1:n.7687-55A=
XR_949152.2:n.7687-55A=
NM_001035.3:c.7343-55A= MANE Select NP_001026.2:n.7343-55A=