Canonical Allele Identifier: CA2335054971

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38503126_38503127delinsAT , CM000681.2:g.38503126_38503127delinsAT	GRCh38
NC_000019.9:g.38993766_38993767delinsAT , CM000681.1:g.38993766_38993767delinsAT	GRCh37
NC_000019.8:g.43685606_43685607delinsAT	NCBI36
NG_008866.1:g.74427_74428delinsAT , LRG_766:g.74427_74428delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7926+156_7926+157delinsAT	ENSP00000471601.2:n.7926+156_7926+157delinsAT
ENST00000359596.8:c.7926+156_7926+157delinsAT MANE Select	ENSP00000352608.2:n.7926+156_7926+157delinsAT
ENST00000355481.8:c.7926+156_7926+157delinsAT	ENSP00000347667.3:n.7926+156_7926+157delinsAT
ENST00000359596.7:c.7926+156_7926+157delinsAT	ENSP00000352608.2:n.7926+156_7926+157delinsAT
ENST00000360985.7:c.7923+156_7923+157delinsAT	ENSP00000354254.4:n.7923+156_7923+157delinsAT
ENST00000594335.5:c.1378+156_1378+157delinsAT
NM_000540.2:c.7926+156_7926+157delinsAT , LRG_766t1:c.7926+156_7926+157delinsAT	NP_000531.2:n.7926+156_7926+157delinsAT
NM_001042723.1:c.7926+156_7926+157delinsAT	NP_001036188.1:n.7926+156_7926+157delinsAT
XM_006723317.1:c.7926+156_7926+157delinsAT	XP_006723380.1:n.7926+156_7926+157delinsAT
XM_006723319.1:c.7926+156_7926+157delinsAT	XP_006723382.1:n.7926+156_7926+157delinsAT
XM_011527204.1:c.7923+156_7923+157delinsAT	XP_011525506.1:n.7923+156_7923+157delinsAT
XM_011527205.1:c.7926+156_7926+157delinsAT	XP_011525507.1:n.7926+156_7926+157delinsAT
XM_006723317.2:c.7926+156_7926+157delinsAT	XP_006723380.1:n.7926+156_7926+157delinsAT
XM_006723319.2:c.7926+156_7926+157delinsAT	XP_006723382.1:n.7926+156_7926+157delinsAT
XM_011527205.2:c.7926+156_7926+157delinsAT	XP_011525507.1:n.7926+156_7926+157delinsAT
XR_001753735.1:n.8009+156_8009+157delinsAT
NM_000540.3:c.7926+156_7926+157delinsAT MANE Select	NP_000531.2:n.7926+156_7926+157delinsAT
NM_001042723.2:c.7926+156_7926+157delinsAT	NP_001036188.1:n.7926+156_7926+157delinsAT