Canonical Allele Identifier: CA2335058728

Gene: RYR1

Linked Data

• dbSNP Id: rs1970672368

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38510367del , CM000681.2:g.38510367del	GRCh38
NC_000019.9:g.39001007del , CM000681.1:g.39001007del	GRCh37
NC_000019.8:g.43692847del	NCBI36
NG_008866.1:g.81668del , LRG_766:g.81668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.8933-131del	ENSP00000471601.2:n.8933-131del
ENST00000359596.8:c.8933-131del MANE Select	ENSP00000352608.2:n.8933-131del
ENST00000355481.8:c.8933-131del	ENSP00000347667.3:n.8933-131del
ENST00000359596.7:c.8933-131del	ENSP00000352608.2:n.8933-131del
ENST00000360985.7:c.8930-131del	ENSP00000354254.4:n.8930-131del
ENST00000594335.5:c.2385-131del
NM_000540.2:c.8933-131del , LRG_766t1:c.8933-131del	NP_000531.2:n.8933-131del
NM_001042723.1:c.8933-131del	NP_001036188.1:n.8933-131del
XM_006723317.1:c.8933-131del	XP_006723380.1:n.8933-131del
XM_006723319.1:c.8933-131del	XP_006723382.1:n.8933-131del
XM_011527204.1:c.8930-131del	XP_011525506.1:n.8930-131del
XM_011527205.1:c.8933-131del	XP_011525507.1:n.8933-131del
XM_006723317.2:c.8933-131del	XP_006723380.1:n.8933-131del
XM_006723319.2:c.8933-131del	XP_006723382.1:n.8933-131del
XM_011527205.2:c.8933-131del	XP_011525507.1:n.8933-131del
XR_001753735.1:n.9016-131del
NM_000540.3:c.8933-131del MANE Select	NP_000531.2:n.8933-131del
NM_001042723.2:c.8933-131del	NP_001036188.1:n.8933-131del