Canonical Allele Identifier: CA405677589
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.38995997A>T (hg19) chr19:g.38505357A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38505357A>T , CM000681.2:g.38505357A>T GRCh38
NC_000019.9:g.38995997A>T , CM000681.1:g.38995997A>T GRCh37
NC_000019.8:g.43687837A>T NCBI36
NG_008866.1:g.76658A>T , LRG_766:g.76658A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.8359A>T ENSP00000471601.2:p.Thr2787Ser
ENST00000359596.8:c.8359A>T MANE Select ENSP00000352608.2:p.Thr2787Ser
ENST00000355481.8:c.8359A>T ENSP00000347667.3:p.Thr2787Ser
ENST00000359596.7:c.8359A>T ENSP00000352608.2:p.Thr2787Ser
ENST00000360985.7:c.8356A>T ENSP00000354254.4:p.Thr2786Ser
ENST00000594335.5:c.1811A>T
NM_000540.2:c.8359A>T , LRG_766t1:c.8359A>T NP_000531.2:p.Thr2787Ser
NM_001042723.1:c.8359A>T NP_001036188.1:p.Thr2787Ser
XM_006723317.1:c.8359A>T XP_006723380.1:p.Thr2787Ser
XM_006723319.1:c.8359A>T XP_006723382.1:p.Thr2787Ser
XM_011527204.1:c.8356A>T XP_011525506.1:p.Thr2786Ser
XM_011527205.1:c.8359A>T XP_011525507.1:p.Thr2787Ser
XM_006723317.2:c.8359A>T XP_006723380.1:p.Thr2787Ser
XM_006723319.2:c.8359A>T XP_006723382.1:p.Thr2787Ser
XM_011527205.2:c.8359A>T XP_011525507.1:p.Thr2787Ser
XR_001753735.1:n.8442A>T
NM_000540.3:c.8359A>T MANE Select NP_000531.2:p.Thr2787Ser
NM_001042723.2:c.8359A>T NP_001036188.1:p.Thr2787Ser
Search 100 bp 5'
Search 100 bp 3'