Canonical Allele Identifier: CA2335092491
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580452A= , CM000681.2:g.38580452A= GRCh38
NC_000019.9:g.39071092A= , CM000681.1:g.39071092A= GRCh37
NC_000019.8:g.43762932A= NCBI36
NG_008866.1:g.151753A= , LRG_766:g.151753A=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1530A=
ENST00000688602.1:c.2927A=
ENST00000689936.1:c.2899A=
ENST00000359596.8:c.14594A= MANE Select ENSP00000352608.2:p.Asn4865=
ENST00000355481.8:c.14579A= ENSP00000347667.3:p.Asn4860=
ENST00000359596.7:c.14594A= ENSP00000352608.2:p.Asn4865=
ENST00000360985.7:c.14576A= ENSP00000354254.4:p.Asn4859=
NM_000540.2:c.14594A= , LRG_766t1:c.14594A= NP_000531.2:p.Asn4865=
NM_001042723.1:c.14579A= NP_001036188.1:p.Asn4860=
XM_006723317.1:c.14576A= XP_006723380.1:p.Asn4859=
XM_006723319.1:c.14561A= XP_006723382.1:p.Asn4854=
XM_011527204.1:c.14591A= XP_011525506.1:p.Asn4864=
XM_011527205.1:c.14507A= XP_011525507.1:p.Asn4836=
XM_006723317.2:c.14576A= XP_006723380.1:p.Asn4859=
XM_006723319.2:c.14561A= XP_006723382.1:p.Asn4854=
XM_011527205.2:c.14507A= XP_011525507.1:p.Asn4836=
NM_000540.3:c.14594A= MANE Select NP_000531.2:p.Asn4865=
NM_001042723.2:c.14579A= NP_001036188.1:p.Asn4860=