Canonical Allele Identifier: CA405673565

Gene: RYR1

Linked Data

• ClinVar Variation Id: 1484529
• ClinVar RCV Id: RCV002005869
• dbSNP Id: rs2145619973
• gnomAD v4: 19-38502890-C-T
• MyVariant Identifiers: chr19:g.38993530C>T (hg19) ; chr19:g.38502890C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38502890C>T , CM000681.2:g.38502890C>T	GRCh38
NC_000019.9:g.38993530C>T , CM000681.1:g.38993530C>T	GRCh37
NC_000019.8:g.43685370C>T	NCBI36
NG_008866.1:g.74191C>T , LRG_766:g.74191C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000599547.6:c.7846C>T	ENSP00000471601.2:p.Pro2616Ser
ENST00000359596.8:c.7846C>T MANE Select	ENSP00000352608.2:p.Pro2616Ser
ENST00000355481.8:c.7846C>T	ENSP00000347667.3:p.Pro2616Ser
ENST00000359596.7:c.7846C>T	ENSP00000352608.2:p.Pro2616Ser
ENST00000360985.7:c.7843C>T	ENSP00000354254.4:p.Pro2615Ser
ENST00000594335.5:c.1298C>T
NM_000540.2:c.7846C>T , LRG_766t1:c.7846C>T	NP_000531.2:p.Pro2616Ser
NM_001042723.1:c.7846C>T	NP_001036188.1:p.Pro2616Ser
XM_006723317.1:c.7846C>T	XP_006723380.1:p.Pro2616Ser
XM_006723319.1:c.7846C>T	XP_006723382.1:p.Pro2616Ser
XM_011527204.1:c.7843C>T	XP_011525506.1:p.Pro2615Ser
XM_011527205.1:c.7846C>T	XP_011525507.1:p.Pro2616Ser
XM_006723317.2:c.7846C>T	XP_006723380.1:p.Pro2616Ser
XM_006723319.2:c.7846C>T	XP_006723382.1:p.Pro2616Ser
XM_011527205.2:c.7846C>T	XP_011525507.1:p.Pro2616Ser
XR_001753735.1:n.7929C>T
NM_000540.3:c.7846C>T MANE Select	NP_000531.2:p.Pro2616Ser
NM_001042723.2:c.7846C>T	NP_001036188.1:p.Pro2616Ser