Canonical Allele Identifier: CA405662223
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38543625A>T , CM000681.2:g.38543625A>T GRCh38
NC_000019.9:g.39034265A>T , CM000681.1:g.39034265A>T GRCh37
NC_000019.8:g.43726105A>T NCBI36
NG_008866.1:g.114926A>T , LRG_766:g.114926A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000688602.1:c.282A>T
ENST00000689936.1:c.264A>T
ENST00000359596.8:c.11872A>T MANE Select ENSP00000352608.2:p.Lys3958Ter
ENST00000355481.8:c.11857A>T ENSP00000347667.3:p.Lys3953Ter
ENST00000359596.7:c.11872A>T ENSP00000352608.2:p.Lys3958Ter
ENST00000360985.7:c.11854A>T ENSP00000354254.4:p.Lys3952Ter
ENST00000593322.1:c.481A>T
ENST00000594335.5:c.5241A>T
NM_000540.2:c.11872A>T , LRG_766t1:c.11872A>T NP_000531.2:p.Lys3958Ter
NM_001042723.1:c.11857A>T NP_001036188.1:p.Lys3953Ter
XM_006723317.1:c.11854A>T XP_006723380.1:p.Lys3952Ter
XM_006723319.1:c.11839A>T XP_006723382.1:p.Lys3947Ter
XM_011527204.1:c.11869A>T XP_011525506.1:p.Lys3957Ter
XM_011527205.1:c.11872A>T XP_011525507.1:p.Lys3958Ter
XM_006723317.2:c.11854A>T XP_006723380.1:p.Lys3952Ter
XM_006723319.2:c.11839A>T XP_006723382.1:p.Lys3947Ter
XM_011527205.2:c.11872A>T XP_011525507.1:p.Lys3958Ter
NM_000540.3:c.11872A>T MANE Select NP_000531.2:p.Lys3958Ter
NM_001042723.2:c.11857A>T NP_001036188.1:p.Lys3953Ter