Canonical Allele Identifier: CA2335092444
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580377T= , CM000681.2:g.38580377T= GRCh38
NC_000019.9:g.39071017T= , CM000681.1:g.39071017T= GRCh37
NC_000019.8:g.43762857T= NCBI36
NG_008866.1:g.151678T= , LRG_766:g.151678T=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1455T=
ENST00000688602.1:c.2852T=
ENST00000689936.1:c.2824T=
ENST00000359596.8:c.14519T= MANE Select ENSP00000352608.2:p.Met4840=
ENST00000355481.8:c.14504T= ENSP00000347667.3:p.Met4835=
ENST00000359596.7:c.14519T= ENSP00000352608.2:p.Met4840=
ENST00000360985.7:c.14501T= ENSP00000354254.4:p.Met4834=
NM_000540.2:c.14519T= , LRG_766t1:c.14519T= NP_000531.2:p.Met4840=
NM_001042723.1:c.14504T= NP_001036188.1:p.Met4835=
XM_006723317.1:c.14501T= XP_006723380.1:p.Met4834=
XM_006723319.1:c.14486T= XP_006723382.1:p.Met4829=
XM_011527204.1:c.14516T= XP_011525506.1:p.Met4839=
XM_011527205.1:c.14432T= XP_011525507.1:p.Met4811=
XM_006723317.2:c.14501T= XP_006723380.1:p.Met4834=
XM_006723319.2:c.14486T= XP_006723382.1:p.Met4829=
XM_011527205.2:c.14432T= XP_011525507.1:p.Met4811=
NM_000540.3:c.14519T= MANE Select NP_000531.2:p.Met4840=
NM_001042723.2:c.14504T= NP_001036188.1:p.Met4835=