Canonical Allele Identifier: CA2335074311

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543372G= , CM000681.2:g.38543372G=	GRCh38
NC_000019.9:g.39034012G= , CM000681.1:g.39034012G=	GRCh37
NC_000019.8:g.43725852G=	NCBI36
NG_008866.1:g.114673G= , LRG_766:g.114673G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.125G=
ENST00000689936.1:c.107G=
ENST00000359596.8:c.11715G= MANE Select	ENSP00000352608.2:p.Gln3905=
ENST00000355481.8:c.11700G=	ENSP00000347667.3:p.Gln3900=
ENST00000359596.7:c.11715G=	ENSP00000352608.2:p.Gln3905=
ENST00000360985.7:c.11697G=	ENSP00000354254.4:p.Gln3899=
ENST00000593322.1:c.324G=
ENST00000594335.5:c.5084G=
NM_000540.2:c.11715G= , LRG_766t1:c.11715G=	NP_000531.2:p.Gln3905=
NM_001042723.1:c.11700G=	NP_001036188.1:p.Gln3900=
XM_006723317.1:c.11697G=	XP_006723380.1:p.Gln3899=
XM_006723319.1:c.11682G=	XP_006723382.1:p.Gln3894=
XM_011527204.1:c.11712G=	XP_011525506.1:p.Gln3904=
XM_011527205.1:c.11715G=	XP_011525507.1:p.Gln3905=
XM_006723317.2:c.11697G=	XP_006723380.1:p.Gln3899=
XM_006723319.2:c.11682G=	XP_006723382.1:p.Gln3894=
XM_011527205.2:c.11715G=	XP_011525507.1:p.Gln3905=
NM_000540.3:c.11715G= MANE Select	NP_000531.2:p.Gln3905=
NM_001042723.2:c.11700G=	NP_001036188.1:p.Gln3900=