Canonical Allele Identifier: CA405672125
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.38993315C>G (hg19) chr19:g.38502675C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502675C>G , CM000681.2:g.38502675C>G GRCh38
NC_000019.9:g.38993315C>G , CM000681.1:g.38993315C>G GRCh37
NC_000019.8:g.43685155C>G NCBI36
NG_008866.1:g.73976C>G , LRG_766:g.73976C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7783C>G ENSP00000471601.2:p.Leu2595Val
ENST00000359596.8:c.7783C>G MANE Select ENSP00000352608.2:p.Leu2595Val
ENST00000355481.8:c.7783C>G ENSP00000347667.3:p.Leu2595Val
ENST00000359596.7:c.7783C>G ENSP00000352608.2:p.Leu2595Val
ENST00000360985.7:c.7780C>G ENSP00000354254.4:p.Leu2594Val
ENST00000594335.5:c.1235C>G
NM_000540.2:c.7783C>G , LRG_766t1:c.7783C>G NP_000531.2:p.Leu2595Val
NM_001042723.1:c.7783C>G NP_001036188.1:p.Leu2595Val
XM_006723317.1:c.7783C>G XP_006723380.1:p.Leu2595Val
XM_006723319.1:c.7783C>G XP_006723382.1:p.Leu2595Val
XM_011527204.1:c.7780C>G XP_011525506.1:p.Leu2594Val
XM_011527205.1:c.7783C>G XP_011525507.1:p.Leu2595Val
XM_006723317.2:c.7783C>G XP_006723380.1:p.Leu2595Val
XM_006723319.2:c.7783C>G XP_006723382.1:p.Leu2595Val
XM_011527205.2:c.7783C>G XP_011525507.1:p.Leu2595Val
XR_001753735.1:n.7866C>G
NM_000540.3:c.7783C>G MANE Select NP_000531.2:p.Leu2595Val
NM_001042723.2:c.7783C>G NP_001036188.1:p.Leu2595Val
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