Canonical Allele Identifier: CA2335084861

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565399G= , CM000681.2:g.38565399G=	GRCh38
NC_000019.9:g.39056039G= , CM000681.1:g.39056039G=	GRCh37
NC_000019.8:g.43747879G=	NCBI36
NG_008866.1:g.136700G= , LRG_766:g.136700G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1G=
ENST00000688602.1:c.1475G=
ENST00000689936.1:c.1457G=
ENST00000359596.8:c.13065G= MANE Select	ENSP00000352608.2:p.Leu4355=
ENST00000355481.8:c.13050G=	ENSP00000347667.3:p.Leu4350=
ENST00000359596.7:c.13065G=	ENSP00000352608.2:p.Leu4355=
ENST00000360985.7:c.13047G=	ENSP00000354254.4:p.Leu4349=
NM_000540.2:c.13065G= , LRG_766t1:c.13065G=	NP_000531.2:p.Leu4355=
NM_001042723.1:c.13050G=	NP_001036188.1:p.Leu4350=
XM_006723317.1:c.13047G=	XP_006723380.1:p.Leu4349=
XM_006723319.1:c.13032G=	XP_006723382.1:p.Leu4344=
XM_011527204.1:c.13062G=	XP_011525506.1:p.Leu4354=
XM_011527205.1:c.13065G=	XP_011525507.1:p.Leu4355=
XM_006723317.2:c.13047G=	XP_006723380.1:p.Leu4349=
XM_006723319.2:c.13032G=	XP_006723382.1:p.Leu4344=
XM_011527205.2:c.13065G=	XP_011525507.1:p.Leu4355=
NM_000540.3:c.13065G= MANE Select	NP_000531.2:p.Leu4355=
NM_001042723.2:c.13050G=	NP_001036188.1:p.Leu4350=