Canonical Allele Identifier: CA405661099

Gene: RYR1

Linked Data

• ClinVar Variation Id: 1328673
• ClinVar RCV Id: RCV001797305
• dbSNP Id: rs2145774604
• MyVariant Identifiers: chr19:g.39033995A>T (hg19) ; chr19:g.38543355A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543355A>T , CM000681.2:g.38543355A>T	GRCh38
NC_000019.9:g.39033995A>T , CM000681.1:g.39033995A>T	GRCh37
NC_000019.8:g.43725835A>T	NCBI36
NG_008866.1:g.114656A>T , LRG_766:g.114656A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.108A>T
ENST00000689936.1:c.90A>T
ENST00000359596.8:c.11698A>T MANE Select	ENSP00000352608.2:p.Asn3900Tyr
ENST00000355481.8:c.11683A>T	ENSP00000347667.3:p.Asn3895Tyr
ENST00000359596.7:c.11698A>T	ENSP00000352608.2:p.Asn3900Tyr
ENST00000360985.7:c.11680A>T	ENSP00000354254.4:p.Asn3894Tyr
ENST00000593322.1:c.307A>T
ENST00000594335.5:c.5067A>T
NM_000540.2:c.11698A>T , LRG_766t1:c.11698A>T	NP_000531.2:p.Asn3900Tyr
NM_001042723.1:c.11683A>T	NP_001036188.1:p.Asn3895Tyr
XM_006723317.1:c.11680A>T	XP_006723380.1:p.Asn3894Tyr
XM_006723319.1:c.11665A>T	XP_006723382.1:p.Asn3889Tyr
XM_011527204.1:c.11695A>T	XP_011525506.1:p.Asn3899Tyr
XM_011527205.1:c.11698A>T	XP_011525507.1:p.Asn3900Tyr
XM_006723317.2:c.11680A>T	XP_006723380.1:p.Asn3894Tyr
XM_006723319.2:c.11665A>T	XP_006723382.1:p.Asn3889Tyr
XM_011527205.2:c.11698A>T	XP_011525507.1:p.Asn3900Tyr
NM_000540.3:c.11698A>T MANE Select	NP_000531.2:p.Asn3900Tyr
NM_001042723.2:c.11683A>T	NP_001036188.1:p.Asn3895Tyr