Canonical Allele Identifier: CA2335092498

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580464A= , CM000681.2:g.38580464A=	GRCh38
NC_000019.9:g.39071104A= , CM000681.1:g.39071104A=	GRCh37
NC_000019.8:g.43762944A=	NCBI36
NG_008866.1:g.151765A= , LRG_766:g.151765A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1542A=
ENST00000688602.1:c.2939A=
ENST00000689936.1:c.2911A=
ENST00000359596.8:c.14606A= MANE Select	ENSP00000352608.2:p.Asp4869=
ENST00000355481.8:c.14591A=	ENSP00000347667.3:p.Asp4864=
ENST00000359596.7:c.14606A=	ENSP00000352608.2:p.Asp4869=
ENST00000360985.7:c.14588A=	ENSP00000354254.4:p.Asp4863=
NM_000540.2:c.14606A= , LRG_766t1:c.14606A=	NP_000531.2:p.Asp4869=
NM_001042723.1:c.14591A=	NP_001036188.1:p.Asp4864=
XM_006723317.1:c.14588A=	XP_006723380.1:p.Asp4863=
XM_006723319.1:c.14573A=	XP_006723382.1:p.Asp4858=
XM_011527204.1:c.14603A=	XP_011525506.1:p.Asp4868=
XM_011527205.1:c.14519A=	XP_011525507.1:p.Asp4840=
XM_006723317.2:c.14588A=	XP_006723380.1:p.Asp4863=
XM_006723319.2:c.14573A=	XP_006723382.1:p.Asp4858=
XM_011527205.2:c.14519A=	XP_011525507.1:p.Asp4840=
NM_000540.3:c.14606A= MANE Select	NP_000531.2:p.Asp4869=
NM_001042723.2:c.14591A=	NP_001036188.1:p.Asp4864=