Canonical Allele Identifier: CA2335092463
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580413A= , CM000681.2:g.38580413A= GRCh38
NC_000019.9:g.39071053A= , CM000681.1:g.39071053A= GRCh37
NC_000019.8:g.43762893A= NCBI36
NG_008866.1:g.151714A= , LRG_766:g.151714A=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1491A=
ENST00000688602.1:c.2888A=
ENST00000689936.1:c.2860A=
ENST00000359596.8:c.14555A= MANE Select ENSP00000352608.2:p.Tyr4852=
ENST00000355481.8:c.14540A= ENSP00000347667.3:p.Tyr4847=
ENST00000359596.7:c.14555A= ENSP00000352608.2:p.Tyr4852=
ENST00000360985.7:c.14537A= ENSP00000354254.4:p.Tyr4846=
NM_000540.2:c.14555A= , LRG_766t1:c.14555A= NP_000531.2:p.Tyr4852=
NM_001042723.1:c.14540A= NP_001036188.1:p.Tyr4847=
XM_006723317.1:c.14537A= XP_006723380.1:p.Tyr4846=
XM_006723319.1:c.14522A= XP_006723382.1:p.Tyr4841=
XM_011527204.1:c.14552A= XP_011525506.1:p.Tyr4851=
XM_011527205.1:c.14468A= XP_011525507.1:p.Tyr4823=
XM_006723317.2:c.14537A= XP_006723380.1:p.Tyr4846=
XM_006723319.2:c.14522A= XP_006723382.1:p.Tyr4841=
XM_011527205.2:c.14468A= XP_011525507.1:p.Tyr4823=
NM_000540.3:c.14555A= MANE Select NP_000531.2:p.Tyr4852=
NM_001042723.2:c.14540A= NP_001036188.1:p.Tyr4847=