Canonical Allele Identifier: CA2335084920

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565508C= , CM000681.2:g.38565508C=	GRCh38
NC_000019.9:g.39056148C= , CM000681.1:g.39056148C=	GRCh37
NC_000019.8:g.43747988C=	NCBI36
NG_008866.1:g.136809C= , LRG_766:g.136809C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.110C=
ENST00000688602.1:c.1584C=
ENST00000689936.1:c.1566C=
ENST00000359596.8:c.13174C= MANE Select	ENSP00000352608.2:p.His4392=
ENST00000355481.8:c.13159C=	ENSP00000347667.3:p.His4387=
ENST00000359596.7:c.13174C=	ENSP00000352608.2:p.His4392=
ENST00000360985.7:c.13156C=	ENSP00000354254.4:p.His4386=
NM_000540.2:c.13174C= , LRG_766t1:c.13174C=	NP_000531.2:p.His4392=
NM_001042723.1:c.13159C=	NP_001036188.1:p.His4387=
XM_006723317.1:c.13156C=	XP_006723380.1:p.His4386=
XM_006723319.1:c.13141C=	XP_006723382.1:p.His4381=
XM_011527204.1:c.13171C=	XP_011525506.1:p.His4391=
XM_011527205.1:c.13174C=	XP_011525507.1:p.His4392=
XM_006723317.2:c.13156C=	XP_006723380.1:p.His4386=
XM_006723319.2:c.13141C=	XP_006723382.1:p.His4381=
XM_011527205.2:c.13174C=	XP_011525507.1:p.His4392=
NM_000540.3:c.13174C= MANE Select	NP_000531.2:p.His4392=
NM_001042723.2:c.13159C=	NP_001036188.1:p.His4387=