Canonical Allele Identifier: CA2335074576

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543912G= , CM000681.2:g.38543912G=	GRCh38
NC_000019.9:g.39034552G= , CM000681.1:g.39034552G=	GRCh37
NC_000019.8:g.43726392G=	NCBI36
NG_008866.1:g.115213G= , LRG_766:g.115213G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.422+37G=
ENST00000689936.1:c.404+37G=
ENST00000359596.8:c.12012+37G= MANE Select	ENSP00000352608.2:n.12012+37G=
ENST00000355481.8:c.11997+37G=	ENSP00000347667.3:n.11997+37G=
ENST00000359596.7:c.12012+37G=	ENSP00000352608.2:n.12012+37G=
ENST00000360985.7:c.11994+37G=	ENSP00000354254.4:n.11994+37G=
ENST00000593322.1:c.621+37G=
ENST00000594335.5:c.5381+37G=
NM_000540.2:c.12012+37G= , LRG_766t1:c.12012+37G=	NP_000531.2:n.12012+37G=
NM_001042723.1:c.11997+37G=	NP_001036188.1:n.11997+37G=
XM_006723317.1:c.11994+37G=	XP_006723380.1:n.11994+37G=
XM_006723319.1:c.11979+37G=	XP_006723382.1:n.11979+37G=
XM_011527204.1:c.12009+37G=	XP_011525506.1:n.12009+37G=
XM_011527205.1:c.12012+37G=	XP_011525507.1:n.12012+37G=
XM_006723317.2:c.11994+37G=	XP_006723380.1:n.11994+37G=
XM_006723319.2:c.11979+37G=	XP_006723382.1:n.11979+37G=
XM_011527205.2:c.12012+37G=	XP_011525507.1:n.12012+37G=
NM_000540.3:c.12012+37G= MANE Select	NP_000531.2:n.12012+37G=
NM_001042723.2:c.11997+37G=	NP_001036188.1:n.11997+37G=