Canonical Allele Identifier: CA2335084881

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565445G= , CM000681.2:g.38565445G=	GRCh38
NC_000019.9:g.39056085G= , CM000681.1:g.39056085G=	GRCh37
NC_000019.8:g.43747925G=	NCBI36
NG_008866.1:g.136746G= , LRG_766:g.136746G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.47G=
ENST00000688602.1:c.1521G=
ENST00000689936.1:c.1503G=
ENST00000359596.8:c.13111G= MANE Select	ENSP00000352608.2:p.Ala4371=
ENST00000355481.8:c.13096G=	ENSP00000347667.3:p.Ala4366=
ENST00000359596.7:c.13111G=	ENSP00000352608.2:p.Ala4371=
ENST00000360985.7:c.13093G=	ENSP00000354254.4:p.Ala4365=
NM_000540.2:c.13111G= , LRG_766t1:c.13111G=	NP_000531.2:p.Ala4371=
NM_001042723.1:c.13096G=	NP_001036188.1:p.Ala4366=
XM_006723317.1:c.13093G=	XP_006723380.1:p.Ala4365=
XM_006723319.1:c.13078G=	XP_006723382.1:p.Ala4360=
XM_011527204.1:c.13108G=	XP_011525506.1:p.Ala4370=
XM_011527205.1:c.13111G=	XP_011525507.1:p.Ala4371=
XM_006723317.2:c.13093G=	XP_006723380.1:p.Ala4365=
XM_006723319.2:c.13078G=	XP_006723382.1:p.Ala4360=
XM_011527205.2:c.13111G=	XP_011525507.1:p.Ala4371=
NM_000540.3:c.13111G= MANE Select	NP_000531.2:p.Ala4371=
NM_001042723.2:c.13096G=	NP_001036188.1:p.Ala4366=