Canonical Allele Identifier: CA405681169

Gene: RYR1

Linked Data

• ClinVar Variation Id: 3072198
• ClinVar RCV Id: RCV004012228
• MyVariant Identifiers: chr19:g.39062839G>T (hg19) ; chr19:g.38572199G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572199G>T , CM000681.2:g.38572199G>T	GRCh38
NC_000019.9:g.39062839G>T , CM000681.1:g.39062839G>T	GRCh37
NC_000019.8:g.43754679G>T	NCBI36
NG_008866.1:g.143500G>T , LRG_766:g.143500G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.863G>T
ENST00000688602.1:c.2260G>T
ENST00000689936.1:c.2232G>T
ENST00000359596.8:c.13927G>T MANE Select	ENSP00000352608.2:p.Ala4643Ser
ENST00000355481.8:c.13912G>T	ENSP00000347667.3:p.Ala4638Ser
ENST00000359596.7:c.13927G>T	ENSP00000352608.2:p.Ala4643Ser
ENST00000360985.7:c.13909G>T	ENSP00000354254.4:p.Ala4637Ser
ENST00000593677.1:c.387G>T
NM_000540.2:c.13927G>T , LRG_766t1:c.13927G>T	NP_000531.2:p.Ala4643Ser
NM_001042723.1:c.13912G>T	NP_001036188.1:p.Ala4638Ser
XM_006723317.1:c.13909G>T	XP_006723380.1:p.Ala4637Ser
XM_006723319.1:c.13894G>T	XP_006723382.1:p.Ala4632Ser
XM_011527204.1:c.13924G>T	XP_011525506.1:p.Ala4642Ser
XM_011527205.1:c.13840G>T	XP_011525507.1:p.Ala4614Ser
XM_006723317.2:c.13909G>T	XP_006723380.1:p.Ala4637Ser
XM_006723319.2:c.13894G>T	XP_006723382.1:p.Ala4632Ser
XM_011527205.2:c.13840G>T	XP_011525507.1:p.Ala4614Ser
NM_000540.3:c.13927G>T MANE Select	NP_000531.2:p.Ala4643Ser
NM_001042723.2:c.13912G>T	NP_001036188.1:p.Ala4638Ser