Canonical Allele Identifier: CA2335092440

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580370C= , CM000681.2:g.38580370C=	GRCh38
NC_000019.9:g.39071010C= , CM000681.1:g.39071010C=	GRCh37
NC_000019.8:g.43762850C=	NCBI36
NG_008866.1:g.151671C= , LRG_766:g.151671C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1448C=
ENST00000688602.1:c.2845C=
ENST00000689936.1:c.2817C=
ENST00000359596.8:c.14512C= MANE Select	ENSP00000352608.2:p.Leu4838=
ENST00000355481.8:c.14497C=	ENSP00000347667.3:p.Leu4833=
ENST00000359596.7:c.14512C=	ENSP00000352608.2:p.Leu4838=
ENST00000360985.7:c.14494C=	ENSP00000354254.4:p.Leu4832=
NM_000540.2:c.14512C= , LRG_766t1:c.14512C=	NP_000531.2:p.Leu4838=
NM_001042723.1:c.14497C=	NP_001036188.1:p.Leu4833=
XM_006723317.1:c.14494C=	XP_006723380.1:p.Leu4832=
XM_006723319.1:c.14479C=	XP_006723382.1:p.Leu4827=
XM_011527204.1:c.14509C=	XP_011525506.1:p.Leu4837=
XM_011527205.1:c.14425C=	XP_011525507.1:p.Leu4809=
XM_006723317.2:c.14494C=	XP_006723380.1:p.Leu4832=
XM_006723319.2:c.14479C=	XP_006723382.1:p.Leu4827=
XM_011527205.2:c.14425C=	XP_011525507.1:p.Leu4809=
NM_000540.3:c.14512C= MANE Select	NP_000531.2:p.Leu4838=
NM_001042723.2:c.14497C=	NP_001036188.1:p.Leu4833=