Canonical Allele Identifier: CA2335084912

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565495C= , CM000681.2:g.38565495C=	GRCh38
NC_000019.9:g.39056135C= , CM000681.1:g.39056135C=	GRCh37
NC_000019.8:g.43747975C=	NCBI36
NG_008866.1:g.136796C= , LRG_766:g.136796C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.97C=
ENST00000688602.1:c.1571C=
ENST00000689936.1:c.1553C=
ENST00000359596.8:c.13161C= MANE Select	ENSP00000352608.2:p.Thr4387=
ENST00000355481.8:c.13146C=	ENSP00000347667.3:p.Thr4382=
ENST00000359596.7:c.13161C=	ENSP00000352608.2:p.Thr4387=
ENST00000360985.7:c.13143C=	ENSP00000354254.4:p.Thr4381=
NM_000540.2:c.13161C= , LRG_766t1:c.13161C=	NP_000531.2:p.Thr4387=
NM_001042723.1:c.13146C=	NP_001036188.1:p.Thr4382=
XM_006723317.1:c.13143C=	XP_006723380.1:p.Thr4381=
XM_006723319.1:c.13128C=	XP_006723382.1:p.Thr4376=
XM_011527204.1:c.13158C=	XP_011525506.1:p.Thr4386=
XM_011527205.1:c.13161C=	XP_011525507.1:p.Thr4387=
XM_006723317.2:c.13143C=	XP_006723380.1:p.Thr4381=
XM_006723319.2:c.13128C=	XP_006723382.1:p.Thr4376=
XM_011527205.2:c.13161C=	XP_011525507.1:p.Thr4387=
NM_000540.3:c.13161C= MANE Select	NP_000531.2:p.Thr4387=
NM_001042723.2:c.13146C=	NP_001036188.1:p.Thr4382=