Canonical Allele Identifier: CA405682538
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39063924G>A (hg19) chr19:g.38573284G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573284G>A , CM000681.2:g.38573284G>A GRCh38
NC_000019.9:g.39063924G>A , CM000681.1:g.39063924G>A GRCh37
NC_000019.8:g.43755764G>A NCBI36
NG_008866.1:g.144585G>A , LRG_766:g.144585G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1042G>A
ENST00000688602.1:c.2439G>A
ENST00000689936.1:c.2411G>A
ENST00000359596.8:c.14106G>A MANE Select ENSP00000352608.2:p.Trp4702Ter
ENST00000355481.8:c.14091G>A ENSP00000347667.3:p.Trp4697Ter
ENST00000359596.7:c.14106G>A ENSP00000352608.2:p.Trp4702Ter
ENST00000360985.7:c.14088G>A ENSP00000354254.4:p.Trp4696Ter
NM_000540.2:c.14106G>A , LRG_766t1:c.14106G>A NP_000531.2:p.Trp4702Ter
NM_001042723.1:c.14091G>A NP_001036188.1:p.Trp4697Ter
XM_006723317.1:c.14088G>A XP_006723380.1:p.Trp4696Ter
XM_006723319.1:c.14073G>A XP_006723382.1:p.Trp4691Ter
XM_011527204.1:c.14103G>A XP_011525506.1:p.Trp4701Ter
XM_011527205.1:c.14019G>A XP_011525507.1:p.Trp4673Ter
XM_006723317.2:c.14088G>A XP_006723380.1:p.Trp4696Ter
XM_006723319.2:c.14073G>A XP_006723382.1:p.Trp4691Ter
XM_011527205.2:c.14019G>A XP_011525507.1:p.Trp4673Ter
NM_000540.3:c.14106G>A MANE Select NP_000531.2:p.Trp4702Ter
NM_001042723.2:c.14091G>A NP_001036188.1:p.Trp4697Ter
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