Canonical Allele Identifier: CA2335094812

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38584731C= , CM000681.2:g.38584731C=	GRCh38
NC_000019.9:g.39075371C= , CM000681.1:g.39075371C=	GRCh37
NC_000019.8:g.43767211C=	NCBI36
NG_008866.1:g.156032C= , LRG_766:g.156032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1583-212C=
ENST00000688602.1:c.2980-212C=
ENST00000689936.1:c.2952-212C=
ENST00000359596.8:c.14647-212C= MANE Select	ENSP00000352608.2:n.14647-212C=
ENST00000355481.8:c.14632-212C=	ENSP00000347667.3:n.14632-212C=
ENST00000359596.7:c.14647-212C=	ENSP00000352608.2:n.14647-212C=
ENST00000360985.7:c.14629-212C=	ENSP00000354254.4:n.14629-212C=
NM_000540.2:c.14647-212C= , LRG_766t1:c.14647-212C=	NP_000531.2:n.14647-212C=
NM_001042723.1:c.14632-212C=	NP_001036188.1:n.14632-212C=
XM_006723317.1:c.14629-212C=	XP_006723380.1:n.14629-212C=
XM_006723319.1:c.14614-212C=	XP_006723382.1:n.14614-212C=
XM_011527204.1:c.14644-212C=	XP_011525506.1:n.14644-212C=
XM_011527205.1:c.14560-212C=	XP_011525507.1:n.14560-212C=
XM_006723317.2:c.14629-212C=	XP_006723380.1:n.14629-212C=
XM_006723319.2:c.14614-212C=	XP_006723382.1:n.14614-212C=
XM_011527205.2:c.14560-212C=	XP_011525507.1:n.14560-212C=
NM_000540.3:c.14647-212C= MANE Select	NP_000531.2:n.14647-212C=
NM_001042723.2:c.14632-212C=	NP_001036188.1:n.14632-212C=