Canonical Allele Identifier: CA2335052911

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38499742G= , CM000681.2:g.38499742G=	GRCh38
NC_000019.9:g.38990382G= , CM000681.1:g.38990382G=	GRCh37
NC_000019.8:g.43682222G=	NCBI36
NG_008866.1:g.71043G= , LRG_766:g.71043G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7135G=	ENSP00000471601.2:p.Ala2379=
ENST00000359596.8:c.7135G= MANE Select	ENSP00000352608.2:p.Ala2379=
ENST00000355481.8:c.7135G=	ENSP00000347667.3:p.Ala2379=
ENST00000359596.7:c.7135G=	ENSP00000352608.2:p.Ala2379=
ENST00000360985.7:c.7132G=	ENSP00000354254.4:p.Ala2378=
ENST00000594335.5:c.587G=
NM_000540.2:c.7135G= , LRG_766t1:c.7135G=	NP_000531.2:p.Ala2379=
NM_001042723.1:c.7135G=	NP_001036188.1:p.Ala2379=
XM_006723317.1:c.7135G=	XP_006723380.1:p.Ala2379=
XM_006723319.1:c.7135G=	XP_006723382.1:p.Ala2379=
XM_011527204.1:c.7132G=	XP_011525506.1:p.Ala2378=
XM_011527205.1:c.7135G=	XP_011525507.1:p.Ala2379=
XM_006723317.2:c.7135G=	XP_006723380.1:p.Ala2379=
XM_006723319.2:c.7135G=	XP_006723382.1:p.Ala2379=
XM_011527205.2:c.7135G=	XP_011525507.1:p.Ala2379=
XR_001753735.1:n.7218G=
NM_000540.3:c.7135G= MANE Select	NP_000531.2:p.Ala2379=
NM_001042723.2:c.7135G=	NP_001036188.1:p.Ala2379=