Canonical Allele Identifier: CA2584911017

Gene: RYR1

Linked Data

• gnomAD v4: 19-38580149-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580149T>C , CM000681.2:g.38580149T>C	GRCh38
NC_000019.9:g.39070789T>C , CM000681.1:g.39070789T>C	GRCh37
NC_000019.8:g.43762629T>C	NCBI36
NG_008866.1:g.151450T>C , LRG_766:g.151450T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1447+21T>C
ENST00000688602.1:c.2844+21T>C
ENST00000689936.1:c.2816+21T>C
ENST00000359596.8:c.14511+21T>C MANE Select	ENSP00000352608.2:n.14511+21T>C
ENST00000355481.8:c.14496+21T>C	ENSP00000347667.3:n.14496+21T>C
ENST00000359596.7:c.14511+21T>C	ENSP00000352608.2:n.14511+21T>C
ENST00000360985.7:c.14493+21T>C	ENSP00000354254.4:n.14493+21T>C
NM_000540.2:c.14511+21T>C , LRG_766t1:c.14511+21T>C	NP_000531.2:n.14511+21T>C
NM_001042723.1:c.14496+21T>C	NP_001036188.1:n.14496+21T>C
XM_006723317.1:c.14493+21T>C	XP_006723380.1:n.14493+21T>C
XM_006723319.1:c.14478+21T>C	XP_006723382.1:n.14478+21T>C
XM_011527204.1:c.14508+21T>C	XP_011525506.1:n.14508+21T>C
XM_011527205.1:c.14424+21T>C	XP_011525507.1:n.14424+21T>C
XM_006723317.2:c.14493+21T>C	XP_006723380.1:n.14493+21T>C
XM_006723319.2:c.14478+21T>C	XP_006723382.1:n.14478+21T>C
XM_011527205.2:c.14424+21T>C	XP_011525507.1:n.14424+21T>C
NM_000540.3:c.14511+21T>C MANE Select	NP_000531.2:n.14511+21T>C
NM_001042723.2:c.14496+21T>C	NP_001036188.1:n.14496+21T>C