Canonical Allele Identifier: CA405679435

Gene: RYR1

Linked Data

• ClinVar Variation Id: 3070935
• ClinVar RCV Id: RCV004014437
• dbSNP Id: rs1568438505
• MyVariant Identifiers: chr19:g.38937141C>T (hg19) ; chr19:g.38446501C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38446501C>T , CM000681.2:g.38446501C>T	GRCh38
NC_000019.9:g.38937141C>T , CM000681.1:g.38937141C>T	GRCh37
NC_000019.8:g.43628981C>T	NCBI36
NG_008866.1:g.17802C>T , LRG_766:g.17802C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.661C>T	ENSP00000471601.2:p.Leu221Phe
ENST00000359596.8:c.661C>T MANE Select	ENSP00000352608.2:p.Leu221Phe
ENST00000355481.8:c.661C>T	ENSP00000347667.3:p.Leu221Phe
ENST00000359596.7:c.661C>T	ENSP00000352608.2:p.Leu221Phe
ENST00000360985.7:c.661C>T	ENSP00000354254.4:p.Leu221Phe
NM_000540.2:c.661C>T , LRG_766t1:c.661C>T	NP_000531.2:p.Leu221Phe
NM_001042723.1:c.661C>T	NP_001036188.1:p.Leu221Phe
XM_006723317.1:c.661C>T	XP_006723380.1:p.Leu221Phe
XM_006723319.1:c.661C>T	XP_006723382.1:p.Leu221Phe
XM_011527204.1:c.661C>T	XP_011525506.1:p.Leu221Phe
XM_011527205.1:c.661C>T	XP_011525507.1:p.Leu221Phe
XM_006723317.2:c.661C>T	XP_006723380.1:p.Leu221Phe
XM_006723319.2:c.661C>T	XP_006723382.1:p.Leu221Phe
XM_011527205.2:c.661C>T	XP_011525507.1:p.Leu221Phe
XR_001753735.1:n.744C>T
NM_000540.3:c.661C>T MANE Select	NP_000531.2:p.Leu221Phe
NM_001042723.2:c.661C>T	NP_001036188.1:p.Leu221Phe