Canonical Allele Identifier: CA2335088981
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573215C= , CM000681.2:g.38573215C= GRCh38
NC_000019.9:g.39063855C= , CM000681.1:g.39063855C= GRCh37
NC_000019.8:g.43755695C= NCBI36
NG_008866.1:g.144516C= , LRG_766:g.144516C=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.973C=
ENST00000688602.1:c.2370C=
ENST00000689936.1:c.2342C=
ENST00000359596.8:c.14037C= MANE Select ENSP00000352608.2:p.Ala4679=
ENST00000355481.8:c.14022C= ENSP00000347667.3:p.Ala4674=
ENST00000359596.7:c.14037C= ENSP00000352608.2:p.Ala4679=
ENST00000360985.7:c.14019C= ENSP00000354254.4:p.Ala4673=
NM_000540.2:c.14037C= , LRG_766t1:c.14037C= NP_000531.2:p.Ala4679=
NM_001042723.1:c.14022C= NP_001036188.1:p.Ala4674=
XM_006723317.1:c.14019C= XP_006723380.1:p.Ala4673=
XM_006723319.1:c.14004C= XP_006723382.1:p.Ala4668=
XM_011527204.1:c.14034C= XP_011525506.1:p.Ala4678=
XM_011527205.1:c.13950C= XP_011525507.1:p.Ala4650=
XM_006723317.2:c.14019C= XP_006723380.1:p.Ala4673=
XM_006723319.2:c.14004C= XP_006723382.1:p.Ala4668=
XM_011527205.2:c.13950C= XP_011525507.1:p.Ala4650=
NM_000540.3:c.14037C= MANE Select NP_000531.2:p.Ala4679=
NM_001042723.2:c.14022C= NP_001036188.1:p.Ala4674=