Canonical Allele Identifier: CA405687839

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071086T>G (hg19) ; chr19:g.38580446T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580446T>G , CM000681.2:g.38580446T>G	GRCh38
NC_000019.9:g.39071086T>G , CM000681.1:g.39071086T>G	GRCh37
NC_000019.8:g.43762926T>G	NCBI36
NG_008866.1:g.151747T>G , LRG_766:g.151747T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1524T>G
ENST00000688602.1:c.2921T>G
ENST00000689936.1:c.2893T>G
ENST00000359596.8:c.14588T>G MANE Select	ENSP00000352608.2:p.Phe4863Cys
ENST00000355481.8:c.14573T>G	ENSP00000347667.3:p.Phe4858Cys
ENST00000359596.7:c.14588T>G	ENSP00000352608.2:p.Phe4863Cys
ENST00000360985.7:c.14570T>G	ENSP00000354254.4:p.Phe4857Cys
NM_000540.2:c.14588T>G , LRG_766t1:c.14588T>G	NP_000531.2:p.Phe4863Cys
NM_001042723.1:c.14573T>G	NP_001036188.1:p.Phe4858Cys
XM_006723317.1:c.14570T>G	XP_006723380.1:p.Phe4857Cys
XM_006723319.1:c.14555T>G	XP_006723382.1:p.Phe4852Cys
XM_011527204.1:c.14585T>G	XP_011525506.1:p.Phe4862Cys
XM_011527205.1:c.14501T>G	XP_011525507.1:p.Phe4834Cys
XM_006723317.2:c.14570T>G	XP_006723380.1:p.Phe4857Cys
XM_006723319.2:c.14555T>G	XP_006723382.1:p.Phe4852Cys
XM_011527205.2:c.14501T>G	XP_011525507.1:p.Phe4834Cys
NM_000540.3:c.14588T>G MANE Select	NP_000531.2:p.Phe4863Cys
NM_001042723.2:c.14573T>G	NP_001036188.1:p.Phe4858Cys