Canonical Allele Identifier: CA405683488

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39001200G>A (hg19) ; chr19:g.38510560G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38510560G>A , CM000681.2:g.38510560G>A	GRCh38
NC_000019.9:g.39001200G>A , CM000681.1:g.39001200G>A	GRCh37
NC_000019.8:g.43693040G>A	NCBI36
NG_008866.1:g.81861G>A , LRG_766:g.81861G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.8995G>A	ENSP00000471601.2:p.Ala2999Thr
ENST00000359596.8:c.8995G>A MANE Select	ENSP00000352608.2:p.Ala2999Thr
ENST00000355481.8:c.8995G>A	ENSP00000347667.3:p.Ala2999Thr
ENST00000359596.7:c.8995G>A	ENSP00000352608.2:p.Ala2999Thr
ENST00000360985.7:c.8992G>A	ENSP00000354254.4:p.Ala2998Thr
ENST00000594335.5:c.2447G>A
NM_000540.2:c.8995G>A , LRG_766t1:c.8995G>A	NP_000531.2:p.Ala2999Thr
NM_001042723.1:c.8995G>A	NP_001036188.1:p.Ala2999Thr
XM_006723317.1:c.8995G>A	XP_006723380.1:p.Ala2999Thr
XM_006723319.1:c.8995G>A	XP_006723382.1:p.Ala2999Thr
XM_011527204.1:c.8992G>A	XP_011525506.1:p.Ala2998Thr
XM_011527205.1:c.8995G>A	XP_011525507.1:p.Ala2999Thr
XM_006723317.2:c.8995G>A	XP_006723380.1:p.Ala2999Thr
XM_006723319.2:c.8995G>A	XP_006723382.1:p.Ala2999Thr
XM_011527205.2:c.8995G>A	XP_011525507.1:p.Ala2999Thr
XR_001753735.1:n.9078G>A
NM_000540.3:c.8995G>A MANE Select	NP_000531.2:p.Ala2999Thr
NM_001042723.2:c.8995G>A	NP_001036188.1:p.Ala2999Thr