Canonical Allele Identifier: CA405653051

Gene: RYR1

Linked Data

• ClinVar Variation Id: 3070974
• ClinVar RCV Id: RCV004014476
• gnomAD v4: 19-38485666-G-T
• MyVariant Identifiers: chr19:g.38976306G>T (hg19) ; chr19:g.38485666G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38485666G>T , CM000681.2:g.38485666G>T	GRCh38
NC_000019.9:g.38976306G>T , CM000681.1:g.38976306G>T	GRCh37
NC_000019.8:g.43668146G>T	NCBI36
NG_008866.1:g.56967G>T , LRG_766:g.56967G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.5011G>T	ENSP00000471601.2:p.Ala1671Ser
ENST00000359596.8:c.5011G>T MANE Select	ENSP00000352608.2:p.Ala1671Ser
ENST00000355481.8:c.5011G>T	ENSP00000347667.3:p.Ala1671Ser
ENST00000359596.7:c.5011G>T	ENSP00000352608.2:p.Ala1671Ser
ENST00000360985.7:c.5008G>T	ENSP00000354254.4:p.Ala1670Ser
NM_000540.2:c.5011G>T , LRG_766t1:c.5011G>T	NP_000531.2:p.Ala1671Ser
NM_001042723.1:c.5011G>T	NP_001036188.1:p.Ala1671Ser
XM_006723317.1:c.5011G>T	XP_006723380.1:p.Ala1671Ser
XM_006723319.1:c.5011G>T	XP_006723382.1:p.Ala1671Ser
XM_011527204.1:c.5008G>T	XP_011525506.1:p.Ala1670Ser
XM_011527205.1:c.5011G>T	XP_011525507.1:p.Ala1671Ser
XM_006723317.2:c.5011G>T	XP_006723380.1:p.Ala1671Ser
XM_006723319.2:c.5011G>T	XP_006723382.1:p.Ala1671Ser
XM_011527205.2:c.5011G>T	XP_011525507.1:p.Ala1671Ser
XR_001753735.1:n.5094G>T
NM_000540.3:c.5011G>T MANE Select	NP_000531.2:p.Ala1671Ser
NM_001042723.2:c.5011G>T	NP_001036188.1:p.Ala1671Ser