Canonical Allele Identifier: CA2335059549

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38512153G= , CM000681.2:g.38512153G=	GRCh38
NC_000019.9:g.39002793G= , CM000681.1:g.39002793G=	GRCh37
NC_000019.8:g.43694633G=	NCBI36
NG_008866.1:g.83454G= , LRG_766:g.83454G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599547.6:c.9173-92G=	ENSP00000471601.2:n.9173-92G=
ENST00000359596.8:c.9233+21G= MANE Select	ENSP00000352608.2:n.9233+21G=
ENST00000355481.8:c.9233+21G=	ENSP00000347667.3:n.9233+21G=
ENST00000359596.7:c.9233+21G=	ENSP00000352608.2:n.9233+21G=
ENST00000360985.7:c.9230+21G=	ENSP00000354254.4:n.9230+21G=
ENST00000594335.5:c.2635+21G=
ENST00000599547.5:c.41-92G=
NM_000540.2:c.9233+21G= , LRG_766t1:c.9233+21G=	NP_000531.2:n.9233+21G=
NM_001042723.1:c.9233+21G=	NP_001036188.1:n.9233+21G=
XM_006723317.1:c.9233+21G=	XP_006723380.1:n.9233+21G=
XM_006723319.1:c.9233+21G=	XP_006723382.1:n.9233+21G=
XM_011527204.1:c.9230+21G=	XP_011525506.1:n.9230+21G=
XM_011527205.1:c.9233+21G=	XP_011525507.1:n.9233+21G=
XM_006723317.2:c.9233+21G=	XP_006723380.1:n.9233+21G=
XM_006723319.2:c.9233+21G=	XP_006723382.1:n.9233+21G=
XM_011527205.2:c.9233+21G=	XP_011525507.1:n.9233+21G=
XR_001753735.1:n.9266+21G=
NM_000540.3:c.9233+21G= MANE Select	NP_000531.2:n.9233+21G=
NM_001042723.2:c.9233+21G=	NP_001036188.1:n.9233+21G=