Canonical Allele Identifier: CA405692631

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39076738G>A (hg19) ; chr19:g.38586098G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38586098G>A , CM000681.2:g.38586098G>A	GRCh38
NC_000019.9:g.39076738G>A , CM000681.1:g.39076738G>A	GRCh37
NC_000019.8:g.43768578G>A	NCBI36
NG_008866.1:g.157399G>A , LRG_766:g.157399G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1812G>A
ENST00000688602.1:c.3209G>A
ENST00000689936.1:c.3181G>A
ENST00000692547.1:n.269G>A
ENST00000359596.8:c.14876G>A MANE Select	ENSP00000352608.2:p.Cys4959Tyr
ENST00000355481.8:c.14861G>A	ENSP00000347667.3:p.Cys4954Tyr
ENST00000359596.7:c.14876G>A	ENSP00000352608.2:p.Cys4959Tyr
ENST00000360985.7:c.14858G>A	ENSP00000354254.4:p.Cys4953Tyr
NM_000540.2:c.14876G>A , LRG_766t1:c.14876G>A	NP_000531.2:p.Cys4959Tyr
NM_001042723.1:c.14861G>A	NP_001036188.1:p.Cys4954Tyr
XM_006723317.1:c.14858G>A	XP_006723380.1:p.Cys4953Tyr
XM_006723319.1:c.14843G>A	XP_006723382.1:p.Cys4948Tyr
XM_011527204.1:c.14873G>A	XP_011525506.1:p.Cys4958Tyr
XM_011527205.1:c.14789G>A	XP_011525507.1:p.Cys4930Tyr
XM_006723317.2:c.14858G>A	XP_006723380.1:p.Cys4953Tyr
XM_006723319.2:c.14843G>A	XP_006723382.1:p.Cys4948Tyr
XM_011527205.2:c.14789G>A	XP_011525507.1:p.Cys4930Tyr
NM_000540.3:c.14876G>A MANE Select	NP_000531.2:p.Cys4959Tyr
NM_001042723.2:c.14861G>A	NP_001036188.1:p.Cys4954Tyr