Canonical Allele Identifier: CA2335095556

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38586107G= , CM000681.2:g.38586107G=	GRCh38
NC_000019.9:g.39076747G= , CM000681.1:g.39076747G=	GRCh37
NC_000019.8:g.43768587G=	NCBI36
NG_008866.1:g.157408G= , LRG_766:g.157408G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1821G=
ENST00000688602.1:c.3218G=
ENST00000689936.1:c.3190G=
ENST00000692547.1:n.278G=
ENST00000359596.8:c.14885G= MANE Select	ENSP00000352608.2:p.Cys4962=
ENST00000355481.8:c.14870G=	ENSP00000347667.3:p.Cys4957=
ENST00000359596.7:c.14885G=	ENSP00000352608.2:p.Cys4962=
ENST00000360985.7:c.14867G=	ENSP00000354254.4:p.Cys4956=
NM_000540.2:c.14885G= , LRG_766t1:c.14885G=	NP_000531.2:p.Cys4962=
NM_001042723.1:c.14870G=	NP_001036188.1:p.Cys4957=
XM_006723317.1:c.14867G=	XP_006723380.1:p.Cys4956=
XM_006723319.1:c.14852G=	XP_006723382.1:p.Cys4951=
XM_011527204.1:c.14882G=	XP_011525506.1:p.Cys4961=
XM_011527205.1:c.14798G=	XP_011525507.1:p.Cys4933=
XM_006723317.2:c.14867G=	XP_006723380.1:p.Cys4956=
XM_006723319.2:c.14852G=	XP_006723382.1:p.Cys4951=
XM_011527205.2:c.14798G=	XP_011525507.1:p.Cys4933=
NM_000540.3:c.14885G= MANE Select	NP_000531.2:p.Cys4962=
NM_001042723.2:c.14870G=	NP_001036188.1:p.Cys4957=