Canonical Allele Identifier: CA2335027144

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38446581G= , CM000681.2:g.38446581G=	GRCh38
NC_000019.9:g.38937221G= , CM000681.1:g.38937221G=	GRCh37
NC_000019.8:g.43629061G=	NCBI36
NG_008866.1:g.17882G= , LRG_766:g.17882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.725+16G=	ENSP00000471601.2:n.725+16G=
ENST00000359596.8:c.725+16G= MANE Select	ENSP00000352608.2:n.725+16G=
ENST00000355481.8:c.725+16G=	ENSP00000347667.3:n.725+16G=
ENST00000359596.7:c.725+16G=	ENSP00000352608.2:n.725+16G=
ENST00000360985.7:c.725+16G=	ENSP00000354254.4:n.725+16G=
NM_000540.2:c.725+16G= , LRG_766t1:c.725+16G=	NP_000531.2:n.725+16G=
NM_001042723.1:c.725+16G=	NP_001036188.1:n.725+16G=
XM_006723317.1:c.725+16G=	XP_006723380.1:n.725+16G=
XM_006723319.1:c.725+16G=	XP_006723382.1:n.725+16G=
XM_011527204.1:c.725+16G=	XP_011525506.1:n.725+16G=
XM_011527205.1:c.725+16G=	XP_011525507.1:n.725+16G=
XM_006723317.2:c.725+16G=	XP_006723380.1:n.725+16G=
XM_006723319.2:c.725+16G=	XP_006723382.1:n.725+16G=
XM_011527205.2:c.725+16G=	XP_011525507.1:n.725+16G=
XR_001753735.1:n.808+16G=
NM_000540.3:c.725+16G= MANE Select	NP_000531.2:n.725+16G=
NM_001042723.2:c.725+16G=	NP_001036188.1:n.725+16G=