Canonical Allele Identifier: CA2335092483
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580443A= , CM000681.2:g.38580443A= GRCh38
NC_000019.9:g.39071083A= , CM000681.1:g.39071083A= GRCh37
NC_000019.8:g.43762923A= NCBI36
NG_008866.1:g.151744A= , LRG_766:g.151744A=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1521A=
ENST00000688602.1:c.2918A=
ENST00000689936.1:c.2890A=
ENST00000359596.8:c.14585A= MANE Select ENSP00000352608.2:p.Lys4862=
ENST00000355481.8:c.14570A= ENSP00000347667.3:p.Lys4857=
ENST00000359596.7:c.14585A= ENSP00000352608.2:p.Lys4862=
ENST00000360985.7:c.14567A= ENSP00000354254.4:p.Lys4856=
NM_000540.2:c.14585A= , LRG_766t1:c.14585A= NP_000531.2:p.Lys4862=
NM_001042723.1:c.14570A= NP_001036188.1:p.Lys4857=
XM_006723317.1:c.14567A= XP_006723380.1:p.Lys4856=
XM_006723319.1:c.14552A= XP_006723382.1:p.Lys4851=
XM_011527204.1:c.14582A= XP_011525506.1:p.Lys4861=
XM_011527205.1:c.14498A= XP_011525507.1:p.Lys4833=
XM_006723317.2:c.14567A= XP_006723380.1:p.Lys4856=
XM_006723319.2:c.14552A= XP_006723382.1:p.Lys4851=
XM_011527205.2:c.14498A= XP_011525507.1:p.Lys4833=
NM_000540.3:c.14585A= MANE Select NP_000531.2:p.Lys4862=
NM_001042723.2:c.14570A= NP_001036188.1:p.Lys4857=