Canonical Allele Identifier: CA2335027361
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38447068_38447072delinsTAAAG , CM000681.2:g.38447068_38447072delinsTAAAG GRCh38
NC_000019.9:g.38937708_38937712delinsTAAAG , CM000681.1:g.38937708_38937712delinsTAAAG GRCh37
NC_000019.8:g.43629548_43629552delinsTAAAG NCBI36
NG_008866.1:g.18369_18373delinsTAAAG , LRG_766:g.18369_18373delinsTAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.800+300_800+304delinsTAAAG ENSP00000471601.2:n.800+300_800+304delinsTAAAG
ENST00000359596.8:c.800+300_800+304delinsTAAAG MANE Select ENSP00000352608.2:n.800+300_800+304delinsTAAAG
ENST00000355481.8:c.800+300_800+304delinsTAAAG ENSP00000347667.3:n.800+300_800+304delinsTAAAG
ENST00000359596.7:c.800+300_800+304delinsTAAAG ENSP00000352608.2:n.800+300_800+304delinsTAAAG
ENST00000360985.7:c.800+300_800+304delinsTAAAG ENSP00000354254.4:n.800+300_800+304delinsTAAAG
NM_000540.2:c.800+300_800+304delinsTAAAG , LRG_766t1:c.800+300_800+304delinsTAAAG NP_000531.2:n.800+300_800+304delinsTAAAG
NM_001042723.1:c.800+300_800+304delinsTAAAG NP_001036188.1:n.800+300_800+304delinsTAAAG
XM_006723317.1:c.800+300_800+304delinsTAAAG XP_006723380.1:n.800+300_800+304delinsTAAAG
XM_006723319.1:c.800+300_800+304delinsTAAAG XP_006723382.1:n.800+300_800+304delinsTAAAG
XM_011527204.1:c.800+300_800+304delinsTAAAG XP_011525506.1:n.800+300_800+304delinsTAAAG
XM_011527205.1:c.800+300_800+304delinsTAAAG XP_011525507.1:n.800+300_800+304delinsTAAAG
XM_006723317.2:c.800+300_800+304delinsTAAAG XP_006723380.1:n.800+300_800+304delinsTAAAG
XM_006723319.2:c.800+300_800+304delinsTAAAG XP_006723382.1:n.800+300_800+304delinsTAAAG
XM_011527205.2:c.800+300_800+304delinsTAAAG XP_011525507.1:n.800+300_800+304delinsTAAAG
XR_001753735.1:n.883+300_883+304delinsTAAAG
NM_000540.3:c.800+300_800+304delinsTAAAG MANE Select NP_000531.2:n.800+300_800+304delinsTAAAG
NM_001042723.2:c.800+300_800+304delinsTAAAG NP_001036188.1:n.800+300_800+304delinsTAAAG