Canonical Allele Identifier: CA633066229
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1970209146

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502771_38502772insAGCAGGGGCAGG , CM000681.2:g.38502771_38502772insAGCAGGGGCAGG GRCh38
NC_000019.9:g.38993411_38993412insAGCAGGGGCAGG , CM000681.1:g.38993411_38993412insAGCAGGGGCAGG GRCh37
NC_000019.8:g.43685251_43685252insAGCAGGGGCAGG NCBI36
NG_008866.1:g.74072_74073insAGCAGGGGCAGG , LRG_766:g.74072_74073insAGCAGGGGCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+44_7835+45insAGCAGGGGCAGG ENSP00000471601.2:n.7835+44_7835+45insAGCAGGGGCAGG
ENST00000359596.8:c.7835+44_7835+45insAGCAGGGGCAGG MANE Select ENSP00000352608.2:n.7835+44_7835+45insAGCAGGGGCAGG
ENST00000355481.8:c.7835+44_7835+45insAGCAGGGGCAGG ENSP00000347667.3:n.7835+44_7835+45insAGCAGGGGCAGG
ENST00000359596.7:c.7835+44_7835+45insAGCAGGGGCAGG ENSP00000352608.2:n.7835+44_7835+45insAGCAGGGGCAGG
ENST00000360985.7:c.7832+44_7832+45insAGCAGGGGCAGG ENSP00000354254.4:n.7832+44_7832+45insAGCAGGGGCAGG
ENST00000594335.5:c.1287+44_1287+45insAGCAGGGGCAGG
NM_000540.2:c.7835+44_7835+45insAGCAGGGGCAGG , LRG_766t1:c.7835+44_7835+45insAGCAGGGGCAGG NP_000531.2:n.7835+44_7835+45insAGCAGGGGCAGG
NM_001042723.1:c.7835+44_7835+45insAGCAGGGGCAGG NP_001036188.1:n.7835+44_7835+45insAGCAGGGGCAGG
XM_006723317.1:c.7835+44_7835+45insAGCAGGGGCAGG XP_006723380.1:n.7835+44_7835+45insAGCAGGGGCAGG
XM_006723319.1:c.7835+44_7835+45insAGCAGGGGCAGG XP_006723382.1:n.7835+44_7835+45insAGCAGGGGCAGG
XM_011527204.1:c.7832+44_7832+45insAGCAGGGGCAGG XP_011525506.1:n.7832+44_7832+45insAGCAGGGGCAGG
XM_011527205.1:c.7835+44_7835+45insAGCAGGGGCAGG XP_011525507.1:n.7835+44_7835+45insAGCAGGGGCAGG
XM_006723317.2:c.7835+44_7835+45insAGCAGGGGCAGG XP_006723380.1:n.7835+44_7835+45insAGCAGGGGCAGG
XM_006723319.2:c.7835+44_7835+45insAGCAGGGGCAGG XP_006723382.1:n.7835+44_7835+45insAGCAGGGGCAGG
XM_011527205.2:c.7835+44_7835+45insAGCAGGGGCAGG XP_011525507.1:n.7835+44_7835+45insAGCAGGGGCAGG
XR_001753735.1:n.7918+44_7918+45insAGCAGGGGCAGG
NM_000540.3:c.7835+44_7835+45insAGCAGGGGCAGG MANE Select NP_000531.2:n.7835+44_7835+45insAGCAGGGGCAGG
NM_001042723.2:c.7835+44_7835+45insAGCAGGGGCAGG NP_001036188.1:n.7835+44_7835+45insAGCAGGGGCAGG