Canonical Allele Identifier: CA2584911058

Gene: RYR1

Linked Data

• gnomAD v4: 19-38580257-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580261del , CM000681.2:g.38580261del	GRCh38
NC_000019.9:g.39070901del , CM000681.1:g.39070901del	GRCh37
NC_000019.8:g.43762741del	NCBI36
NG_008866.1:g.151562del , LRG_766:g.151562del

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1448-109del
ENST00000688602.1:c.2845-109del
ENST00000689936.1:c.2817-109del
ENST00000359596.8:c.14512-109del MANE Select	ENSP00000352608.2:n.14512-109del
ENST00000355481.8:c.14497-109del	ENSP00000347667.3:n.14497-109del
ENST00000359596.7:c.14512-109del	ENSP00000352608.2:n.14512-109del
ENST00000360985.7:c.14494-109del	ENSP00000354254.4:n.14494-109del
NM_000540.2:c.14512-109del , LRG_766t1:c.14512-109del	NP_000531.2:n.14512-109del
NM_001042723.1:c.14497-109del	NP_001036188.1:n.14497-109del
XM_006723317.1:c.14494-109del	XP_006723380.1:n.14494-109del
XM_006723319.1:c.14479-109del	XP_006723382.1:n.14479-109del
XM_011527204.1:c.14509-109del	XP_011525506.1:n.14509-109del
XM_011527205.1:c.14425-109del	XP_011525507.1:n.14425-109del
XM_006723317.2:c.14494-109del	XP_006723380.1:n.14494-109del
XM_006723319.2:c.14479-109del	XP_006723382.1:n.14479-109del
XM_011527205.2:c.14425-109del	XP_011525507.1:n.14425-109del
NM_000540.3:c.14512-109del MANE Select	NP_000531.2:n.14512-109del
NM_001042723.2:c.14497-109del	NP_001036188.1:n.14497-109del