Canonical Allele Identifier: CA2335025708

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38443517C= , CM000681.2:g.38443517C=	GRCh38
NC_000019.9:g.38934157C= , CM000681.1:g.38934157C=	GRCh37
NC_000019.8:g.43625997C=	NCBI36
NG_008866.1:g.14818C= , LRG_766:g.14818C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599547.6:c.271-41C=	ENSP00000471601.2:n.271-41C=
ENST00000359596.8:c.271-41C= MANE Select	ENSP00000352608.2:n.271-41C=
ENST00000355481.8:c.271-41C=	ENSP00000347667.3:n.271-41C=
ENST00000359596.7:c.271-41C=	ENSP00000352608.2:n.271-41C=
ENST00000360985.7:c.271-41C=	ENSP00000354254.4:n.271-41C=
NM_000540.2:c.271-41C= , LRG_766t1:c.271-41C=	NP_000531.2:n.271-41C=
NM_001042723.1:c.271-41C=	NP_001036188.1:n.271-41C=
XM_006723317.1:c.271-41C=	XP_006723380.1:n.271-41C=
XM_006723319.1:c.271-41C=	XP_006723382.1:n.271-41C=
XM_011527204.1:c.271-41C=	XP_011525506.1:n.271-41C=
XM_011527205.1:c.271-41C=	XP_011525507.1:n.271-41C=
XM_006723317.2:c.271-41C=	XP_006723380.1:n.271-41C=
XM_006723319.2:c.271-41C=	XP_006723382.1:n.271-41C=
XM_011527205.2:c.271-41C=	XP_011525507.1:n.271-41C=
XR_001753735.1:n.354-41C=
NM_000540.3:c.271-41C= MANE Select	NP_000531.2:n.271-41C=
NM_001042723.2:c.271-41C=	NP_001036188.1:n.271-41C=