Canonical Allele Identifier: CA2335092268

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580028A= , CM000681.2:g.38580028A=	GRCh38
NC_000019.9:g.39070668A= , CM000681.1:g.39070668A=	GRCh37
NC_000019.8:g.43762508A=	NCBI36
NG_008866.1:g.151329A= , LRG_766:g.151329A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1347A=
ENST00000688602.1:c.2744A=
ENST00000689936.1:c.2716A=
ENST00000359596.8:c.14411A= MANE Select	ENSP00000352608.2:p.His4804=
ENST00000355481.8:c.14396A=	ENSP00000347667.3:p.His4799=
ENST00000359596.7:c.14411A=	ENSP00000352608.2:p.His4804=
ENST00000360985.7:c.14393A=	ENSP00000354254.4:p.His4798=
NM_000540.2:c.14411A= , LRG_766t1:c.14411A=	NP_000531.2:p.His4804=
NM_001042723.1:c.14396A=	NP_001036188.1:p.His4799=
XM_006723317.1:c.14393A=	XP_006723380.1:p.His4798=
XM_006723319.1:c.14378A=	XP_006723382.1:p.His4793=
XM_011527204.1:c.14408A=	XP_011525506.1:p.His4803=
XM_011527205.1:c.14324A=	XP_011525507.1:p.His4775=
XM_006723317.2:c.14393A=	XP_006723380.1:p.His4798=
XM_006723319.2:c.14378A=	XP_006723382.1:p.His4793=
XM_011527205.2:c.14324A=	XP_011525507.1:p.His4775=
NM_000540.3:c.14411A= MANE Select	NP_000531.2:p.His4804=
NM_001042723.2:c.14396A=	NP_001036188.1:p.His4799=