Canonical Allele Identifier: CA2741629741

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543512A>C , CM000681.2:g.38543512A>C	GRCh38
NC_000019.9:g.39034152A>C , CM000681.1:g.39034152A>C	GRCh37
NC_000019.8:g.43725992A>C	NCBI36
NG_008866.1:g.114813A>C , LRG_766:g.114813A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.189-20A>C
ENST00000689936.1:c.171-20A>C
ENST00000359596.8:c.11779-20A>C MANE Select	ENSP00000352608.2:n.11779-20A>C
ENST00000355481.8:c.11764-20A>C	ENSP00000347667.3:n.11764-20A>C
ENST00000359596.7:c.11779-20A>C	ENSP00000352608.2:n.11779-20A>C
ENST00000360985.7:c.11761-20A>C	ENSP00000354254.4:n.11761-20A>C
ENST00000593322.1:c.388-20A>C
ENST00000594335.5:c.5148-20A>C
NM_000540.2:c.11779-20A>C , LRG_766t1:c.11779-20A>C	NP_000531.2:n.11779-20A>C
NM_001042723.1:c.11764-20A>C	NP_001036188.1:n.11764-20A>C
XM_006723317.1:c.11761-20A>C	XP_006723380.1:n.11761-20A>C
XM_006723319.1:c.11746-20A>C	XP_006723382.1:n.11746-20A>C
XM_011527204.1:c.11776-20A>C	XP_011525506.1:n.11776-20A>C
XM_011527205.1:c.11779-20A>C	XP_011525507.1:n.11779-20A>C
XM_006723317.2:c.11761-20A>C	XP_006723380.1:n.11761-20A>C
XM_006723319.2:c.11746-20A>C	XP_006723382.1:n.11746-20A>C
XM_011527205.2:c.11779-20A>C	XP_011525507.1:n.11779-20A>C
NM_000540.3:c.11779-20A>C MANE Select	NP_000531.2:n.11779-20A>C
NM_001042723.2:c.11764-20A>C	NP_001036188.1:n.11764-20A>C