Canonical Allele Identifier: CA2335051143
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38496241A= , CM000681.2:g.38496241A= GRCh38
NC_000019.9:g.38986881A= , CM000681.1:g.38986881A= GRCh37
NC_000019.8:g.43678721A= NCBI36
NG_008866.1:g.67542A= , LRG_766:g.67542A=

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.6575A= ENSP00000471601.2:p.Tyr2192=
ENST00000359596.8:c.6575A= MANE Select ENSP00000352608.2:p.Tyr2192=
ENST00000355481.8:c.6575A= ENSP00000347667.3:p.Tyr2192=
ENST00000359596.7:c.6575A= ENSP00000352608.2:p.Tyr2192=
ENST00000360985.7:c.6572A= ENSP00000354254.4:p.Tyr2191=
ENST00000594335.5:c.27A=
NM_000540.2:c.6575A= , LRG_766t1:c.6575A= NP_000531.2:p.Tyr2192=
NM_001042723.1:c.6575A= NP_001036188.1:p.Tyr2192=
XM_006723317.1:c.6575A= XP_006723380.1:p.Tyr2192=
XM_006723319.1:c.6575A= XP_006723382.1:p.Tyr2192=
XM_011527204.1:c.6572A= XP_011525506.1:p.Tyr2191=
XM_011527205.1:c.6575A= XP_011525507.1:p.Tyr2192=
XM_006723317.2:c.6575A= XP_006723380.1:p.Tyr2192=
XM_006723319.2:c.6575A= XP_006723382.1:p.Tyr2192=
XM_011527205.2:c.6575A= XP_011525507.1:p.Tyr2192=
XR_001753735.1:n.6658A=
NM_000540.3:c.6575A= MANE Select NP_000531.2:p.Tyr2192=
NM_001042723.2:c.6575A= NP_001036188.1:p.Tyr2192=