Canonical Allele Identifier: CA2335028154

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38448673C= , CM000681.2:g.38448673C=	GRCh38
NC_000019.9:g.38939313C= , CM000681.1:g.38939313C=	GRCh37
NC_000019.8:g.43631153C=	NCBI36
NG_008866.1:g.19974C= , LRG_766:g.19974C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.982C= MANE Select	NP_000531.2:p.Arg328=
ENST00000359596.8:c.982C= MANE Select	ENSP00000352608.2:p.Arg328=
NM_000540.2:c.982C= , LRG_766t1:c.982C=	NP_000531.2:p.Arg328=
NM_001042723.1:c.982C=	NP_001036188.1:p.Arg328=
NM_001042723.2:c.982C=	NP_001036188.1:p.Arg328=
ENST00000355481.8:c.982C=	ENSP00000347667.3:p.Arg328=
ENST00000359596.7:c.982C=	ENSP00000352608.2:p.Arg328=
ENST00000360985.7:c.982C=	ENSP00000354254.4:p.Arg328=
ENST00000599547.6:c.982C=	ENSP00000471601.2:p.Arg328=
XM_006723317.1:c.982C=	XP_006723380.1:p.Arg328=
XM_006723317.2:c.982C=	XP_006723380.1:p.Arg328=
XM_006723319.1:c.982C=	XP_006723382.1:p.Arg328=
XM_006723319.2:c.982C=	XP_006723382.1:p.Arg328=
XM_011527204.1:c.979C=	XP_011525506.1:p.Arg327=
XM_011527205.1:c.982C=	XP_011525507.1:p.Arg328=
XM_011527205.2:c.982C=	XP_011525507.1:p.Arg328=
XR_001753735.1:n.1065C=