Canonical Allele Identifier: CA2335088967
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573181C= , CM000681.2:g.38573181C= GRCh38
NC_000019.9:g.39063821C= , CM000681.1:g.39063821C= GRCh37
NC_000019.8:g.43755661C= NCBI36
NG_008866.1:g.144482C= , LRG_766:g.144482C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.939C=
ENST00000688602.1:c.2336C=
ENST00000689936.1:c.2308C=
ENST00000359596.8:c.14003C= MANE Select ENSP00000352608.2:p.Pro4668=
ENST00000355481.8:c.13988C= ENSP00000347667.3:p.Pro4663=
ENST00000359596.7:c.14003C= ENSP00000352608.2:p.Pro4668=
ENST00000360985.7:c.13985C= ENSP00000354254.4:p.Pro4662=
NM_000540.2:c.14003C= , LRG_766t1:c.14003C= NP_000531.2:p.Pro4668=
NM_001042723.1:c.13988C= NP_001036188.1:p.Pro4663=
XM_006723317.1:c.13985C= XP_006723380.1:p.Pro4662=
XM_006723319.1:c.13970C= XP_006723382.1:p.Pro4657=
XM_011527204.1:c.14000C= XP_011525506.1:p.Pro4667=
XM_011527205.1:c.13916C= XP_011525507.1:p.Pro4639=
XM_006723317.2:c.13985C= XP_006723380.1:p.Pro4662=
XM_006723319.2:c.13970C= XP_006723382.1:p.Pro4657=
XM_011527205.2:c.13916C= XP_011525507.1:p.Pro4639=
NM_000540.3:c.14003C= MANE Select NP_000531.2:p.Pro4668=
NM_001042723.2:c.13988C= NP_001036188.1:p.Pro4663=