Canonical Allele Identifier: CA2335091332
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578032C= , CM000681.2:g.38578032C= GRCh38
NC_000019.9:g.39068672C= , CM000681.1:g.39068672C= GRCh37
NC_000019.8:g.43760512C= NCBI36
NG_008866.1:g.149333C= , LRG_766:g.149333C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1223C=
ENST00000688602.1:c.2620C=
ENST00000689936.1:c.2592C=
ENST00000359596.8:c.14287C= MANE Select ENSP00000352608.2:p.Pro4763=
ENST00000355481.8:c.14272C= ENSP00000347667.3:p.Pro4758=
ENST00000359596.7:c.14287C= ENSP00000352608.2:p.Pro4763=
ENST00000360985.7:c.14269C= ENSP00000354254.4:p.Pro4757=
NM_000540.2:c.14287C= , LRG_766t1:c.14287C= NP_000531.2:p.Pro4763=
NM_001042723.1:c.14272C= NP_001036188.1:p.Pro4758=
XM_006723317.1:c.14269C= XP_006723380.1:p.Pro4757=
XM_006723319.1:c.14254C= XP_006723382.1:p.Pro4752=
XM_011527204.1:c.14284C= XP_011525506.1:p.Pro4762=
XM_011527205.1:c.14200C= XP_011525507.1:p.Pro4734=
XM_006723317.2:c.14269C= XP_006723380.1:p.Pro4757=
XM_006723319.2:c.14254C= XP_006723382.1:p.Pro4752=
XM_011527205.2:c.14200C= XP_011525507.1:p.Pro4734=
NM_000540.3:c.14287C= MANE Select NP_000531.2:p.Pro4763=
NM_001042723.2:c.14272C= NP_001036188.1:p.Pro4758=