Canonical Allele Identifier: CA405685462
Gene: RYR1 HGNC NCBI

Linked Data

gnomAD v4: 19-38578202-A-G
MyVariant Identifiers: chr19:g.39068842A>G (hg19) chr19:g.38578202A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578202A>G , CM000681.2:g.38578202A>G GRCh38
NC_000019.9:g.39068842A>G , CM000681.1:g.39068842A>G GRCh37
NC_000019.8:g.43760682A>G NCBI36
NG_008866.1:g.149503A>G , LRG_766:g.149503A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1298A>G
ENST00000688602.1:c.2695A>G
ENST00000689936.1:c.2667A>G
ENST00000359596.8:c.14362A>G MANE Select ENSP00000352608.2:p.Asn4788Asp
ENST00000355481.8:c.14347A>G ENSP00000347667.3:p.Asn4783Asp
ENST00000359596.7:c.14362A>G ENSP00000352608.2:p.Asn4788Asp
ENST00000360985.7:c.14344A>G ENSP00000354254.4:p.Asn4782Asp
NM_000540.2:c.14362A>G , LRG_766t1:c.14362A>G NP_000531.2:p.Asn4788Asp
NM_001042723.1:c.14347A>G NP_001036188.1:p.Asn4783Asp
XM_006723317.1:c.14344A>G XP_006723380.1:p.Asn4782Asp
XM_006723319.1:c.14329A>G XP_006723382.1:p.Asn4777Asp
XM_011527204.1:c.14359A>G XP_011525506.1:p.Asn4787Asp
XM_011527205.1:c.14275A>G XP_011525507.1:p.Asn4759Asp
XM_006723317.2:c.14344A>G XP_006723380.1:p.Asn4782Asp
XM_006723319.2:c.14329A>G XP_006723382.1:p.Asn4777Asp
XM_011527205.2:c.14275A>G XP_011525507.1:p.Asn4759Asp
NM_000540.3:c.14362A>G MANE Select NP_000531.2:p.Asn4788Asp
NM_001042723.2:c.14347A>G NP_001036188.1:p.Asn4783Asp
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