Canonical Allele Identifier: CA2335084940

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565541G= , CM000681.2:g.38565541G=	GRCh38
NC_000019.9:g.39056181G= , CM000681.1:g.39056181G=	GRCh37
NC_000019.8:g.43748021G=	NCBI36
NG_008866.1:g.136842G= , LRG_766:g.136842G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.143G=
ENST00000688602.1:c.1617G=
ENST00000689936.1:c.1599G=
ENST00000359596.8:c.13207G= MANE Select	ENSP00000352608.2:p.Ala4403=
ENST00000355481.8:c.13192G=	ENSP00000347667.3:p.Ala4398=
ENST00000359596.7:c.13207G=	ENSP00000352608.2:p.Ala4403=
ENST00000360985.7:c.13189G=	ENSP00000354254.4:p.Ala4397=
NM_000540.2:c.13207G= , LRG_766t1:c.13207G=	NP_000531.2:p.Ala4403=
NM_001042723.1:c.13192G=	NP_001036188.1:p.Ala4398=
XM_006723317.1:c.13189G=	XP_006723380.1:p.Ala4397=
XM_006723319.1:c.13174G=	XP_006723382.1:p.Ala4392=
XM_011527204.1:c.13204G=	XP_011525506.1:p.Ala4402=
XM_011527205.1:c.13207G=	XP_011525507.1:p.Ala4403=
XM_006723317.2:c.13189G=	XP_006723380.1:p.Ala4397=
XM_006723319.2:c.13174G=	XP_006723382.1:p.Ala4392=
XM_011527205.2:c.13207G=	XP_011525507.1:p.Ala4403=
NM_000540.3:c.13207G= MANE Select	NP_000531.2:p.Ala4403=
NM_001042723.2:c.13192G=	NP_001036188.1:p.Ala4398=