Canonical Allele Identifier: CA2335089029
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573322C= , CM000681.2:g.38573322C= GRCh38
NC_000019.9:g.39063962C= , CM000681.1:g.39063962C= GRCh37
NC_000019.8:g.43755802C= NCBI36
NG_008866.1:g.144623C= , LRG_766:g.144623C=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1065+15C=
ENST00000688602.1:c.2462+15C=
ENST00000689936.1:c.2434+15C=
ENST00000359596.8:c.14129+15C= MANE Select ENSP00000352608.2:n.14129+15C=
ENST00000355481.8:c.14114+15C= ENSP00000347667.3:n.14114+15C=
ENST00000359596.7:c.14129+15C= ENSP00000352608.2:n.14129+15C=
ENST00000360985.7:c.14111+15C= ENSP00000354254.4:n.14111+15C=
NM_000540.2:c.14129+15C= , LRG_766t1:c.14129+15C= NP_000531.2:n.14129+15C=
NM_001042723.1:c.14114+15C= NP_001036188.1:n.14114+15C=
XM_006723317.1:c.14111+15C= XP_006723380.1:n.14111+15C=
XM_006723319.1:c.14096+15C= XP_006723382.1:n.14096+15C=
XM_011527204.1:c.14126+15C= XP_011525506.1:n.14126+15C=
XM_011527205.1:c.14042+15C= XP_011525507.1:n.14042+15C=
XM_006723317.2:c.14111+15C= XP_006723380.1:n.14111+15C=
XM_006723319.2:c.14096+15C= XP_006723382.1:n.14096+15C=
XM_011527205.2:c.14042+15C= XP_011525507.1:n.14042+15C=
NM_000540.3:c.14129+15C= MANE Select NP_000531.2:n.14129+15C=
NM_001042723.2:c.14114+15C= NP_001036188.1:n.14114+15C=