Canonical Allele Identifier: CA2335091272
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577911T= , CM000681.2:g.38577911T= GRCh38
NC_000019.9:g.39068551T= , CM000681.1:g.39068551T= GRCh37
NC_000019.8:g.43760391T= NCBI36
NG_008866.1:g.149212T= , LRG_766:g.149212T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1109-7T=
ENST00000688602.1:c.2506-7T=
ENST00000689936.1:c.2478-7T=
ENST00000359596.8:c.14173-7T= MANE Select ENSP00000352608.2:n.14173-7T=
ENST00000355481.8:c.14158-7T= ENSP00000347667.3:n.14158-7T=
ENST00000359596.7:c.14173-7T= ENSP00000352608.2:n.14173-7T=
ENST00000360985.7:c.14155-7T= ENSP00000354254.4:n.14155-7T=
NM_000540.2:c.14173-7T= , LRG_766t1:c.14173-7T= NP_000531.2:n.14173-7T=
NM_001042723.1:c.14158-7T= NP_001036188.1:n.14158-7T=
XM_006723317.1:c.14155-7T= XP_006723380.1:n.14155-7T=
XM_006723319.1:c.14140-7T= XP_006723382.1:n.14140-7T=
XM_011527204.1:c.14170-7T= XP_011525506.1:n.14170-7T=
XM_011527205.1:c.14086-7T= XP_011525507.1:n.14086-7T=
XM_006723317.2:c.14155-7T= XP_006723380.1:n.14155-7T=
XM_006723319.2:c.14140-7T= XP_006723382.1:n.14140-7T=
XM_011527205.2:c.14086-7T= XP_011525507.1:n.14086-7T=
NM_000540.3:c.14173-7T= MANE Select NP_000531.2:n.14173-7T=
NM_001042723.2:c.14158-7T= NP_001036188.1:n.14158-7T=