Canonical Allele Identifier: CA2584903380
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38512204T>C , CM000681.2:g.38512204T>C GRCh38
NC_000019.9:g.39002844T>C , CM000681.1:g.39002844T>C GRCh37
NC_000019.8:g.43694684T>C NCBI36
NG_008866.1:g.83505T>C , LRG_766:g.83505T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.9173-41T>C ENSP00000471601.2:n.9173-41T>C
ENST00000359596.8:c.9234-41T>C MANE Select ENSP00000352608.2:n.9234-41T>C
ENST00000355481.8:c.9234-41T>C ENSP00000347667.3:n.9234-41T>C
ENST00000359596.7:c.9234-41T>C ENSP00000352608.2:n.9234-41T>C
ENST00000360985.7:c.9231-41T>C ENSP00000354254.4:n.9231-41T>C
ENST00000594335.5:c.2636-41T>C
ENST00000599547.5:c.41-41T>C
NM_000540.2:c.9234-41T>C , LRG_766t1:c.9234-41T>C NP_000531.2:n.9234-41T>C
NM_001042723.1:c.9234-41T>C NP_001036188.1:n.9234-41T>C
XM_006723317.1:c.9234-41T>C XP_006723380.1:n.9234-41T>C
XM_006723319.1:c.9234-41T>C XP_006723382.1:n.9234-41T>C
XM_011527204.1:c.9231-41T>C XP_011525506.1:n.9231-41T>C
XM_011527205.1:c.9234-41T>C XP_011525507.1:n.9234-41T>C
XM_006723317.2:c.9234-41T>C XP_006723380.1:n.9234-41T>C
XM_006723319.2:c.9234-41T>C XP_006723382.1:n.9234-41T>C
XM_011527205.2:c.9234-41T>C XP_011525507.1:n.9234-41T>C
XR_001753735.1:n.9267-41T>C
NM_000540.3:c.9234-41T>C MANE Select NP_000531.2:n.9234-41T>C
NM_001042723.2:c.9234-41T>C NP_001036188.1:n.9234-41T>C