Canonical Allele Identifier: CA405691098

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39075721C>A (hg19) ; chr19:g.38585081C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38585081C>A , CM000681.2:g.38585081C>A	GRCh38
NC_000019.9:g.39075721C>A , CM000681.1:g.39075721C>A	GRCh37
NC_000019.8:g.43767561C>A	NCBI36
NG_008866.1:g.156382C>A , LRG_766:g.156382C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1721C>A
ENST00000688602.1:c.3118C>A
ENST00000689936.1:c.3090C>A
ENST00000692547.1:n.178C>A
ENST00000359596.8:c.14785C>A MANE Select	ENSP00000352608.2:p.Leu4929Met
ENST00000355481.8:c.14770C>A	ENSP00000347667.3:p.Leu4924Met
ENST00000359596.7:c.14785C>A	ENSP00000352608.2:p.Leu4929Met
ENST00000360985.7:c.14767C>A	ENSP00000354254.4:p.Leu4923Met
NM_000540.2:c.14785C>A , LRG_766t1:c.14785C>A	NP_000531.2:p.Leu4929Met
NM_001042723.1:c.14770C>A	NP_001036188.1:p.Leu4924Met
XM_006723317.1:c.14767C>A	XP_006723380.1:p.Leu4923Met
XM_006723319.1:c.14752C>A	XP_006723382.1:p.Leu4918Met
XM_011527204.1:c.14782C>A	XP_011525506.1:p.Leu4928Met
XM_011527205.1:c.14698C>A	XP_011525507.1:p.Leu4900Met
XM_006723317.2:c.14767C>A	XP_006723380.1:p.Leu4923Met
XM_006723319.2:c.14752C>A	XP_006723382.1:p.Leu4918Met
XM_011527205.2:c.14698C>A	XP_011525507.1:p.Leu4900Met
NM_000540.3:c.14785C>A MANE Select	NP_000531.2:p.Leu4929Met
NM_001042723.2:c.14770C>A	NP_001036188.1:p.Leu4924Met