Canonical Allele Identifier: CA405673990

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565508-C-A
• MyVariant Identifiers: chr19:g.39056148C>A (hg19) ; chr19:g.38565508C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565508C>A , CM000681.2:g.38565508C>A	GRCh38
NC_000019.9:g.39056148C>A , CM000681.1:g.39056148C>A	GRCh37
NC_000019.8:g.43747988C>A	NCBI36
NG_008866.1:g.136809C>A , LRG_766:g.136809C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.110C>A
ENST00000688602.1:c.1584C>A
ENST00000689936.1:c.1566C>A
ENST00000359596.8:c.13174C>A MANE Select	ENSP00000352608.2:p.His4392Asn
ENST00000355481.8:c.13159C>A	ENSP00000347667.3:p.His4387Asn
ENST00000359596.7:c.13174C>A	ENSP00000352608.2:p.His4392Asn
ENST00000360985.7:c.13156C>A	ENSP00000354254.4:p.His4386Asn
NM_000540.2:c.13174C>A , LRG_766t1:c.13174C>A	NP_000531.2:p.His4392Asn
NM_001042723.1:c.13159C>A	NP_001036188.1:p.His4387Asn
XM_006723317.1:c.13156C>A	XP_006723380.1:p.His4386Asn
XM_006723319.1:c.13141C>A	XP_006723382.1:p.His4381Asn
XM_011527204.1:c.13171C>A	XP_011525506.1:p.His4391Asn
XM_011527205.1:c.13174C>A	XP_011525507.1:p.His4392Asn
XM_006723317.2:c.13156C>A	XP_006723380.1:p.His4386Asn
XM_006723319.2:c.13141C>A	XP_006723382.1:p.His4381Asn
XM_011527205.2:c.13174C>A	XP_011525507.1:p.His4392Asn
NM_000540.3:c.13174C>A MANE Select	NP_000531.2:p.His4392Asn
NM_001042723.2:c.13159C>A	NP_001036188.1:p.His4387Asn