Canonical Allele Identifier: CA405684680
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578006A>C , CM000681.2:g.38578006A>C GRCh38
NC_000019.9:g.39068646A>C , CM000681.1:g.39068646A>C GRCh37
NC_000019.8:g.43760486A>C NCBI36
NG_008866.1:g.149307A>C , LRG_766:g.149307A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1197A>C
ENST00000688602.1:c.2594A>C
ENST00000689936.1:c.2566A>C
ENST00000359596.8:c.14261A>C MANE Select ENSP00000352608.2:p.His4754Pro
ENST00000355481.8:c.14246A>C ENSP00000347667.3:p.His4749Pro
ENST00000359596.7:c.14261A>C ENSP00000352608.2:p.His4754Pro
ENST00000360985.7:c.14243A>C ENSP00000354254.4:p.His4748Pro
NM_000540.2:c.14261A>C , LRG_766t1:c.14261A>C NP_000531.2:p.His4754Pro
NM_001042723.1:c.14246A>C NP_001036188.1:p.His4749Pro
XM_006723317.1:c.14243A>C XP_006723380.1:p.His4748Pro
XM_006723319.1:c.14228A>C XP_006723382.1:p.His4743Pro
XM_011527204.1:c.14258A>C XP_011525506.1:p.His4753Pro
XM_011527205.1:c.14174A>C XP_011525507.1:p.His4725Pro
XM_006723317.2:c.14243A>C XP_006723380.1:p.His4748Pro
XM_006723319.2:c.14228A>C XP_006723382.1:p.His4743Pro
XM_011527205.2:c.14174A>C XP_011525507.1:p.His4725Pro
NM_000540.3:c.14261A>C MANE Select NP_000531.2:p.His4754Pro
NM_001042723.2:c.14246A>C NP_001036188.1:p.His4749Pro