Canonical Allele Identifier: CA2335089016

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573288C= , CM000681.2:g.38573288C=	GRCh38
NC_000019.9:g.39063928C= , CM000681.1:g.39063928C=	GRCh37
NC_000019.8:g.43755768C=	NCBI36
NG_008866.1:g.144589C= , LRG_766:g.144589C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1046C=
ENST00000688602.1:c.2443C=
ENST00000689936.1:c.2415C=
ENST00000359596.8:c.14110C= MANE Select	ENSP00000352608.2:p.Arg4704=
ENST00000355481.8:c.14095C=	ENSP00000347667.3:p.Arg4699=
ENST00000359596.7:c.14110C=	ENSP00000352608.2:p.Arg4704=
ENST00000360985.7:c.14092C=	ENSP00000354254.4:p.Arg4698=
NM_000540.2:c.14110C= , LRG_766t1:c.14110C=	NP_000531.2:p.Arg4704=
NM_001042723.1:c.14095C=	NP_001036188.1:p.Arg4699=
XM_006723317.1:c.14092C=	XP_006723380.1:p.Arg4698=
XM_006723319.1:c.14077C=	XP_006723382.1:p.Arg4693=
XM_011527204.1:c.14107C=	XP_011525506.1:p.Arg4703=
XM_011527205.1:c.14023C=	XP_011525507.1:p.Arg4675=
XM_006723317.2:c.14092C=	XP_006723380.1:p.Arg4698=
XM_006723319.2:c.14077C=	XP_006723382.1:p.Arg4693=
XM_011527205.2:c.14023C=	XP_011525507.1:p.Arg4675=
NM_000540.3:c.14110C= MANE Select	NP_000531.2:p.Arg4704=
NM_001042723.2:c.14095C=	NP_001036188.1:p.Arg4699=