Canonical Allele Identifier: CA2335094953

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38584996C= , CM000681.2:g.38584996C=	GRCh38
NC_000019.9:g.39075636C= , CM000681.1:g.39075636C=	GRCh37
NC_000019.8:g.43767476C=	NCBI36
NG_008866.1:g.156297C= , LRG_766:g.156297C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1636C=
ENST00000688602.1:c.3033C=
ENST00000689936.1:c.3005C=
ENST00000692547.1:n.93C=
ENST00000359596.8:c.14700C= MANE Select	ENSP00000352608.2:p.Asp4900=
ENST00000355481.8:c.14685C=	ENSP00000347667.3:p.Asp4895=
ENST00000359596.7:c.14700C=	ENSP00000352608.2:p.Asp4900=
ENST00000360985.7:c.14682C=	ENSP00000354254.4:p.Asp4894=
NM_000540.2:c.14700C= , LRG_766t1:c.14700C=	NP_000531.2:p.Asp4900=
NM_001042723.1:c.14685C=	NP_001036188.1:p.Asp4895=
XM_006723317.1:c.14682C=	XP_006723380.1:p.Asp4894=
XM_006723319.1:c.14667C=	XP_006723382.1:p.Asp4889=
XM_011527204.1:c.14697C=	XP_011525506.1:p.Asp4899=
XM_011527205.1:c.14613C=	XP_011525507.1:p.Asp4871=
XM_006723317.2:c.14682C=	XP_006723380.1:p.Asp4894=
XM_006723319.2:c.14667C=	XP_006723382.1:p.Asp4889=
XM_011527205.2:c.14613C=	XP_011525507.1:p.Asp4871=
NM_000540.3:c.14700C= MANE Select	NP_000531.2:p.Asp4900=
NM_001042723.2:c.14685C=	NP_001036188.1:p.Asp4895=