Canonical Allele Identifier: CA2335070956
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38535986C= , CM000681.2:g.38535986C= GRCh38
NC_000019.9:g.39026626C= , CM000681.1:g.39026626C= GRCh37
NC_000019.8:g.43718466C= NCBI36
NG_008866.1:g.107287C= , LRG_766:g.107287C=

Transcript Alleles

HGVS Amino-acid change
ENST00000359596.8:c.11517-11C= MANE Select ENSP00000352608.2:n.11517-11C=
ENST00000355481.8:c.11502-11C= ENSP00000347667.3:n.11502-11C=
ENST00000359596.7:c.11517-11C= ENSP00000352608.2:n.11517-11C=
ENST00000360985.7:c.11499-11C= ENSP00000354254.4:n.11499-11C=
ENST00000593322.1:c.217+594C=
ENST00000594335.5:c.4904-11C=
ENST00000596431.5:c.246-11C= ENSP00000470848.1:n.246-11C=
ENST00000601514.5:c.798-11C= ENSP00000472497.1:n.798-11C=
NM_000540.2:c.11517-11C= , LRG_766t1:c.11517-11C= NP_000531.2:n.11517-11C=
NM_001042723.1:c.11502-11C= NP_001036188.1:n.11502-11C=
XM_006723317.1:c.11517-11C= XP_006723380.1:n.11517-11C=
XM_006723319.1:c.11502-11C= XP_006723382.1:n.11502-11C=
XM_011527204.1:c.11514-11C= XP_011525506.1:n.11514-11C=
XM_011527205.1:c.11517-11C= XP_011525507.1:n.11517-11C=
XM_006723317.2:c.11517-11C= XP_006723380.1:n.11517-11C=
XM_006723319.2:c.11502-11C= XP_006723382.1:n.11502-11C=
XM_011527205.2:c.11517-11C= XP_011525507.1:n.11517-11C=
NM_000540.3:c.11517-11C= MANE Select NP_000531.2:n.11517-11C=
NM_001042723.2:c.11502-11C= NP_001036188.1:n.11502-11C=