Canonical Allele Identifier: CA405690785

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39075686T>A (hg19) ; chr19:g.38585046T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38585046T>A , CM000681.2:g.38585046T>A	GRCh38
NC_000019.9:g.39075686T>A , CM000681.1:g.39075686T>A	GRCh37
NC_000019.8:g.43767526T>A	NCBI36
NG_008866.1:g.156347T>A , LRG_766:g.156347T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1686T>A
ENST00000688602.1:c.3083T>A
ENST00000689936.1:c.3055T>A
ENST00000692547.1:n.143T>A
ENST00000359596.8:c.14750T>A MANE Select	ENSP00000352608.2:p.Phe4917Tyr
ENST00000355481.8:c.14735T>A	ENSP00000347667.3:p.Phe4912Tyr
ENST00000359596.7:c.14750T>A	ENSP00000352608.2:p.Phe4917Tyr
ENST00000360985.7:c.14732T>A	ENSP00000354254.4:p.Phe4911Tyr
NM_000540.2:c.14750T>A , LRG_766t1:c.14750T>A	NP_000531.2:p.Phe4917Tyr
NM_001042723.1:c.14735T>A	NP_001036188.1:p.Phe4912Tyr
XM_006723317.1:c.14732T>A	XP_006723380.1:p.Phe4911Tyr
XM_006723319.1:c.14717T>A	XP_006723382.1:p.Phe4906Tyr
XM_011527204.1:c.14747T>A	XP_011525506.1:p.Phe4916Tyr
XM_011527205.1:c.14663T>A	XP_011525507.1:p.Phe4888Tyr
XM_006723317.2:c.14732T>A	XP_006723380.1:p.Phe4911Tyr
XM_006723319.2:c.14717T>A	XP_006723382.1:p.Phe4906Tyr
XM_011527205.2:c.14663T>A	XP_011525507.1:p.Phe4888Tyr
NM_000540.3:c.14750T>A MANE Select	NP_000531.2:p.Phe4917Tyr
NM_001042723.2:c.14735T>A	NP_001036188.1:p.Phe4912Tyr