Canonical Allele Identifier: CA405688010

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071119A>T (hg19) ; chr19:g.38580479A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580479A>T , CM000681.2:g.38580479A>T	GRCh38
NC_000019.9:g.39071119A>T , CM000681.1:g.39071119A>T	GRCh37
NC_000019.8:g.43762959A>T	NCBI36
NG_008866.1:g.151780A>T , LRG_766:g.151780A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1557A>T
ENST00000688602.1:c.2954A>T
ENST00000689936.1:c.2926A>T
ENST00000359596.8:c.14621A>T MANE Select	ENSP00000352608.2:p.Asp4874Val
ENST00000355481.8:c.14606A>T	ENSP00000347667.3:p.Asp4869Val
ENST00000359596.7:c.14621A>T	ENSP00000352608.2:p.Asp4874Val
ENST00000360985.7:c.14603A>T	ENSP00000354254.4:p.Asp4868Val
NM_000540.2:c.14621A>T , LRG_766t1:c.14621A>T	NP_000531.2:p.Asp4874Val
NM_001042723.1:c.14606A>T	NP_001036188.1:p.Asp4869Val
XM_006723317.1:c.14603A>T	XP_006723380.1:p.Asp4868Val
XM_006723319.1:c.14588A>T	XP_006723382.1:p.Asp4863Val
XM_011527204.1:c.14618A>T	XP_011525506.1:p.Asp4873Val
XM_011527205.1:c.14534A>T	XP_011525507.1:p.Asp4845Val
XM_006723317.2:c.14603A>T	XP_006723380.1:p.Asp4868Val
XM_006723319.2:c.14588A>T	XP_006723382.1:p.Asp4863Val
XM_011527205.2:c.14534A>T	XP_011525507.1:p.Asp4845Val
NM_000540.3:c.14621A>T MANE Select	NP_000531.2:p.Asp4874Val
NM_001042723.2:c.14606A>T	NP_001036188.1:p.Asp4869Val