Canonical Allele Identifier: CA2335094916
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38584932C= , CM000681.2:g.38584932C= GRCh38
NC_000019.9:g.39075572C= , CM000681.1:g.39075572C= GRCh37
NC_000019.8:g.43767412C= NCBI36
NG_008866.1:g.156233C= , LRG_766:g.156233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1583-11C=
ENST00000688602.1:c.2980-11C=
ENST00000689936.1:c.2952-11C=
ENST00000692547.1:n.29C=
ENST00000359596.8:c.14647-11C= MANE Select ENSP00000352608.2:n.14647-11C=
ENST00000355481.8:c.14632-11C= ENSP00000347667.3:n.14632-11C=
ENST00000359596.7:c.14647-11C= ENSP00000352608.2:n.14647-11C=
ENST00000360985.7:c.14629-11C= ENSP00000354254.4:n.14629-11C=
NM_000540.2:c.14647-11C= , LRG_766t1:c.14647-11C= NP_000531.2:n.14647-11C=
NM_001042723.1:c.14632-11C= NP_001036188.1:n.14632-11C=
XM_006723317.1:c.14629-11C= XP_006723380.1:n.14629-11C=
XM_006723319.1:c.14614-11C= XP_006723382.1:n.14614-11C=
XM_011527204.1:c.14644-11C= XP_011525506.1:n.14644-11C=
XM_011527205.1:c.14560-11C= XP_011525507.1:n.14560-11C=
XM_006723317.2:c.14629-11C= XP_006723380.1:n.14629-11C=
XM_006723319.2:c.14614-11C= XP_006723382.1:n.14614-11C=
XM_011527205.2:c.14560-11C= XP_011525507.1:n.14560-11C=
NM_000540.3:c.14647-11C= MANE Select NP_000531.2:n.14647-11C=
NM_001042723.2:c.14632-11C= NP_001036188.1:n.14632-11C=