Canonical Allele Identifier: CA405690928

Gene: RYR1

Linked Data

• gnomAD v4: 19-38585063-T-A
• MyVariant Identifiers: chr19:g.39075703T>A (hg19) ; chr19:g.38585063T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38585063T>A , CM000681.2:g.38585063T>A	GRCh38
NC_000019.9:g.39075703T>A , CM000681.1:g.39075703T>A	GRCh37
NC_000019.8:g.43767543T>A	NCBI36
NG_008866.1:g.156364T>A , LRG_766:g.156364T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1703T>A
ENST00000688602.1:c.3100T>A
ENST00000689936.1:c.3072T>A
ENST00000692547.1:n.160T>A
ENST00000359596.8:c.14767T>A MANE Select	ENSP00000352608.2:p.Phe4923Ile
ENST00000355481.8:c.14752T>A	ENSP00000347667.3:p.Phe4918Ile
ENST00000359596.7:c.14767T>A	ENSP00000352608.2:p.Phe4923Ile
ENST00000360985.7:c.14749T>A	ENSP00000354254.4:p.Phe4917Ile
NM_000540.2:c.14767T>A , LRG_766t1:c.14767T>A	NP_000531.2:p.Phe4923Ile
NM_001042723.1:c.14752T>A	NP_001036188.1:p.Phe4918Ile
XM_006723317.1:c.14749T>A	XP_006723380.1:p.Phe4917Ile
XM_006723319.1:c.14734T>A	XP_006723382.1:p.Phe4912Ile
XM_011527204.1:c.14764T>A	XP_011525506.1:p.Phe4922Ile
XM_011527205.1:c.14680T>A	XP_011525507.1:p.Phe4894Ile
XM_006723317.2:c.14749T>A	XP_006723380.1:p.Phe4917Ile
XM_006723319.2:c.14734T>A	XP_006723382.1:p.Phe4912Ile
XM_011527205.2:c.14680T>A	XP_011525507.1:p.Phe4894Ile
NM_000540.3:c.14767T>A MANE Select	NP_000531.2:p.Phe4923Ile
NM_001042723.2:c.14752T>A	NP_001036188.1:p.Phe4918Ile