Canonical Allele Identifier: CA081121
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577949G>C , CM000681.2:g.38577949G>C GRCh38
NC_000019.9:g.39068589G>C , CM000681.1:g.39068589G>C GRCh37
NC_000019.8:g.43760429G>C NCBI36
NG_008866.1:g.149250G>C , LRG_766:g.149250G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1140G>C
ENST00000688602.1:c.2537G>C
ENST00000689936.1:c.2509G>C
ENST00000359596.8:c.14204G>C MANE Select ENSP00000352608.2:p.Arg4735Pro
ENST00000355481.8:c.14189G>C ENSP00000347667.3:p.Arg4730Pro
ENST00000359596.7:c.14204G>C ENSP00000352608.2:p.Arg4735Pro
ENST00000360985.7:c.14186G>C ENSP00000354254.4:p.Arg4729Pro
NM_000540.2:c.14204G>C , LRG_766t1:c.14204G>C NP_000531.2:p.Arg4735Pro
NM_001042723.1:c.14189G>C NP_001036188.1:p.Arg4730Pro
XM_006723317.1:c.14186G>C XP_006723380.1:p.Arg4729Pro
XM_006723319.1:c.14171G>C XP_006723382.1:p.Arg4724Pro
XM_011527204.1:c.14201G>C XP_011525506.1:p.Arg4734Pro
XM_011527205.1:c.14117G>C XP_011525507.1:p.Arg4706Pro
XM_006723317.2:c.14186G>C XP_006723380.1:p.Arg4729Pro
XM_006723319.2:c.14171G>C XP_006723382.1:p.Arg4724Pro
XM_011527205.2:c.14117G>C XP_011525507.1:p.Arg4706Pro
NM_000540.3:c.14204G>C MANE Select NP_000531.2:p.Arg4735Pro
NM_001042723.2:c.14189G>C NP_001036188.1:p.Arg4730Pro