Canonical Allele Identifier: CA405692266

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39076601G>A (hg19) ; chr19:g.38585961G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38585961G>A , CM000681.2:g.38585961G>A	GRCh38
NC_000019.9:g.39076601G>A , CM000681.1:g.39076601G>A	GRCh37
NC_000019.8:g.43768441G>A	NCBI36
NG_008866.1:g.157262G>A , LRG_766:g.157262G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1763G>A
ENST00000688602.1:c.3160G>A
ENST00000689936.1:c.3132G>A
ENST00000692547.1:n.220G>A
ENST00000359596.8:c.14827G>A MANE Select	ENSP00000352608.2:p.Glu4943Lys
ENST00000355481.8:c.14812G>A	ENSP00000347667.3:p.Glu4938Lys
ENST00000359596.7:c.14827G>A	ENSP00000352608.2:p.Glu4943Lys
ENST00000360985.7:c.14809G>A	ENSP00000354254.4:p.Glu4937Lys
NM_000540.2:c.14827G>A , LRG_766t1:c.14827G>A	NP_000531.2:p.Glu4943Lys
NM_001042723.1:c.14812G>A	NP_001036188.1:p.Glu4938Lys
XM_006723317.1:c.14809G>A	XP_006723380.1:p.Glu4937Lys
XM_006723319.1:c.14794G>A	XP_006723382.1:p.Glu4932Lys
XM_011527204.1:c.14824G>A	XP_011525506.1:p.Glu4942Lys
XM_011527205.1:c.14740G>A	XP_011525507.1:p.Glu4914Lys
XM_006723317.2:c.14809G>A	XP_006723380.1:p.Glu4937Lys
XM_006723319.2:c.14794G>A	XP_006723382.1:p.Glu4932Lys
XM_011527205.2:c.14740G>A	XP_011525507.1:p.Glu4914Lys
NM_000540.3:c.14827G>A MANE Select	NP_000531.2:p.Glu4943Lys
NM_001042723.2:c.14812G>A	NP_001036188.1:p.Glu4938Lys