Canonical Allele Identifier: CA2814347112
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502802_38502803insACAGGGGCAGGGGCAGGG , CM000681.2:g.38502802_38502803insACAGGGGCAGGGGCAGGG GRCh38
NC_000019.9:g.38993442_38993443insACAGGGGCAGGGGCAGGG , CM000681.1:g.38993442_38993443insACAGGGGCAGGGGCAGGG GRCh37
NC_000019.8:g.43685282_43685283insACAGGGGCAGGGGCAGGG NCBI36
NG_008866.1:g.74103_74104insACAGGGGCAGGGGCAGGG , LRG_766:g.74103_74104insACAGGGGCAGGGGCAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG ENSP00000471601.2:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
ENST00000359596.8:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG MANE Select ENSP00000352608.2:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
ENST00000355481.8:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG ENSP00000347667.3:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
ENST00000359596.7:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG ENSP00000352608.2:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
ENST00000360985.7:c.7832+75_7833-77insACAGGGGCAGGGGCAGGG ENSP00000354254.4:n.7832+75_7833-77insACAGGGGCAGGGGCAGGG
ENST00000594335.5:c.1287+75_1288-77insACAGGGGCAGGGGCAGGG
NM_000540.2:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG , LRG_766t1:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG NP_000531.2:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
NM_001042723.1:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG NP_001036188.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
XM_006723317.1:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG XP_006723380.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
XM_006723319.1:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG XP_006723382.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
XM_011527204.1:c.7832+75_7833-77insACAGGGGCAGGGGCAGGG XP_011525506.1:n.7832+75_7833-77insACAGGGGCAGGGGCAGGG
XM_011527205.1:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG XP_011525507.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
XM_006723317.2:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG XP_006723380.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
XM_006723319.2:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG XP_006723382.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
XM_011527205.2:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG XP_011525507.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
XR_001753735.1:n.7918+75_7919-77insACAGGGGCAGGGGCAGGG
NM_000540.3:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG MANE Select NP_000531.2:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG
NM_001042723.2:c.7835+75_7836-77insACAGGGGCAGGGGCAGGG NP_001036188.1:n.7835+75_7836-77insACAGGGGCAGGGGCAGGG