Canonical Allele Identifier: CA405693351
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38586184A>G , CM000681.2:g.38586184A>G GRCh38
NC_000019.9:g.39076824A>G , CM000681.1:g.39076824A>G GRCh37
NC_000019.8:g.43768664A>G NCBI36
NG_008866.1:g.157485A>G , LRG_766:g.157485A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1898A>G
ENST00000688602.1:c.3295A>G
ENST00000689936.1:c.3267A>G
ENST00000692547.1:n.355A>G
ENST00000359596.8:c.14962A>G MANE Select ENSP00000352608.2:p.Asn4988Asp
ENST00000355481.8:c.14947A>G ENSP00000347667.3:p.Asn4983Asp
ENST00000359596.7:c.14962A>G ENSP00000352608.2:p.Asn4988Asp
ENST00000360985.7:c.14944A>G ENSP00000354254.4:p.Asn4982Asp
NM_000540.2:c.14962A>G , LRG_766t1:c.14962A>G NP_000531.2:p.Asn4988Asp
NM_001042723.1:c.14947A>G NP_001036188.1:p.Asn4983Asp
XM_006723317.1:c.14944A>G XP_006723380.1:p.Asn4982Asp
XM_006723319.1:c.14929A>G XP_006723382.1:p.Asn4977Asp
XM_011527204.1:c.14959A>G XP_011525506.1:p.Asn4987Asp
XM_011527205.1:c.14875A>G XP_011525507.1:p.Asn4959Asp
XM_006723317.2:c.14944A>G XP_006723380.1:p.Asn4982Asp
XM_006723319.2:c.14929A>G XP_006723382.1:p.Asn4977Asp
XM_011527205.2:c.14875A>G XP_011525507.1:p.Asn4959Asp
NM_000540.3:c.14962A>G MANE Select NP_000531.2:p.Asn4988Asp
NM_001042723.2:c.14947A>G NP_001036188.1:p.Asn4983Asp