Canonical Allele Identifier: CA2335088460

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572243C= , CM000681.2:g.38572243C=	GRCh38
NC_000019.9:g.39062883C= , CM000681.1:g.39062883C=	GRCh37
NC_000019.8:g.43754723C=	NCBI36
NG_008866.1:g.143544C= , LRG_766:g.143544C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.907C=
ENST00000688602.1:c.2304C=
ENST00000689936.1:c.2276C=
ENST00000359596.8:c.13971C= MANE Select	ENSP00000352608.2:p.Leu4657=
ENST00000355481.8:c.13956C=	ENSP00000347667.3:p.Leu4652=
ENST00000359596.7:c.13971C=	ENSP00000352608.2:p.Leu4657=
ENST00000360985.7:c.13953C=	ENSP00000354254.4:p.Leu4651=
ENST00000593677.1:c.431C=
NM_000540.2:c.13971C= , LRG_766t1:c.13971C=	NP_000531.2:p.Leu4657=
NM_001042723.1:c.13956C=	NP_001036188.1:p.Leu4652=
XM_006723317.1:c.13953C=	XP_006723380.1:p.Leu4651=
XM_006723319.1:c.13938C=	XP_006723382.1:p.Leu4646=
XM_011527204.1:c.13968C=	XP_011525506.1:p.Leu4656=
XM_011527205.1:c.13884C=	XP_011525507.1:p.Leu4628=
XM_006723317.2:c.13953C=	XP_006723380.1:p.Leu4651=
XM_006723319.2:c.13938C=	XP_006723382.1:p.Leu4646=
XM_011527205.2:c.13884C=	XP_011525507.1:p.Leu4628=
NM_000540.3:c.13971C= MANE Select	NP_000531.2:p.Leu4657=
NM_001042723.2:c.13956C=	NP_001036188.1:p.Leu4652=