Canonical Allele Identifier: CA2335092306

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580112C= , CM000681.2:g.38580112C=	GRCh38
NC_000019.9:g.39070752C= , CM000681.1:g.39070752C=	GRCh37
NC_000019.8:g.43762592C=	NCBI36
NG_008866.1:g.151413C= , LRG_766:g.151413C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.14495C= MANE Select	NP_000531.2:p.Thr4832=
ENST00000359596.8:c.14495C= MANE Select	ENSP00000352608.2:p.Thr4832=
NM_000540.2:c.14495C= , LRG_766t1:c.14495C=	NP_000531.2:p.Thr4832=
NM_001042723.1:c.14480C=	NP_001036188.1:p.Thr4827=
NM_001042723.2:c.14480C=	NP_001036188.1:p.Thr4827=
ENST00000355481.8:c.14480C=	ENSP00000347667.3:p.Thr4827=
ENST00000359596.7:c.14495C=	ENSP00000352608.2:p.Thr4832=
ENST00000360985.7:c.14477C=	ENSP00000354254.4:p.Thr4826=
ENST00000593677.2:c.1431C=
ENST00000688602.1:c.2828C=
ENST00000689936.1:c.2800C=
XM_006723317.1:c.14477C=	XP_006723380.1:p.Thr4826=
XM_006723317.2:c.14477C=	XP_006723380.1:p.Thr4826=
XM_006723319.1:c.14462C=	XP_006723382.1:p.Thr4821=
XM_006723319.2:c.14462C=	XP_006723382.1:p.Thr4821=
XM_011527204.1:c.14492C=	XP_011525506.1:p.Thr4831=
XM_011527205.1:c.14408C=	XP_011525507.1:p.Thr4803=
XM_011527205.2:c.14408C=	XP_011525507.1:p.Thr4803=