Canonical Allele Identifier: CA2487439262

Gene: RYR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237677959T= , CM000663.2:g.237677959T=	GRCh38
NC_000001.10:g.237841259T= , CM000663.1:g.237841259T=	GRCh37
NC_000001.9:g.235907882T=	NCBI36
NG_008799.2:g.640558T=
NG_008799.3:g.640776T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.8831-2497T=	ENSP00000499659.2:n.8831-2497T=
ENST00000659194.3:c.8831-89T=	ENSP00000499653.3:n.8831-89T=
ENST00000660292.2:c.8831-89T=	ENSP00000499787.2:n.8831-89T=
ENST00000659194.2:c.1020-89T=
ENST00000366574.7:c.8831-89T= MANE Select	ENSP00000355533.2:n.8831-89T=
ENST00000659194.1:c.1020-89T=
ENST00000360064.7:c.8783-89T=	ENSP00000353174.7:n.8783-89T=
ENST00000366574.6:c.8831-89T=	ENSP00000355533.2:n.8831-89T=
ENST00000609119.1:n.84-2497T=
NM_001035.2:c.8831-89T=	NP_001026.2:n.8831-89T=
XM_006711802.2:c.8861-89T=	XP_006711865.1:n.8861-89T=
XM_006711803.2:c.8858-89T=	XP_006711866.1:n.8858-89T=
XM_006711804.2:c.8861-89T=	XP_006711867.1:n.8861-89T=
XM_006711805.2:c.8831-89T=	XP_006711868.1:n.8831-89T=
XM_006711806.2:c.8861-89T=	XP_006711869.1:n.8861-89T=
XM_006711807.2:c.8861-89T=	XP_006711870.1:n.8861-89T=
XM_006711808.2:c.8860+3113T=	XP_006711871.1:n.8860+3113T=
XM_006711810.2:c.8828-89T=	XP_006711873.1:n.8828-89T=
XR_949152.1:n.9142-89T=
XM_006711802.3:c.8861-89T=	XP_006711865.1:n.8861-89T=
XM_006711803.3:c.8858-89T=	XP_006711866.1:n.8858-89T=
XM_006711804.3:c.8861-89T=	XP_006711867.1:n.8861-89T=
XM_006711805.3:c.8831-89T=	XP_006711868.1:n.8831-89T=
XM_006711806.3:c.8861-89T=	XP_006711869.1:n.8861-89T=
XM_006711807.3:c.8861-89T=	XP_006711870.1:n.8861-89T=
XM_006711808.3:c.8860+3113T=	XP_006711871.1:n.8860+3113T=
XM_006711810.3:c.8828-89T=	XP_006711873.1:n.8828-89T=
XM_017002028.1:c.8840-89T=	XP_016857517.1:n.8840-89T=
XR_949152.2:n.9175-89T=
NM_001035.3:c.8831-89T= MANE Select	NP_001026.2:n.8831-89T=