Canonical Allele Identifier: CA507356127

Gene: RYR1

Linked Data

• COSMIC: COSM4399348
• MyVariant Identifiers: chr19:g.39071075C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580435C>T , CM000681.2:g.38580435C>T	GRCh38
NC_000019.9:g.39071075C>T , CM000681.1:g.39071075C>T	GRCh37
NC_000019.8:g.43762915C>T	NCBI36
NG_008866.1:g.151736C>T , LRG_766:g.151736C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1513C>T
ENST00000688602.1:c.2910C>T
ENST00000689936.1:c.2882C>T
ENST00000359596.8:c.14577C>T MANE Select	ENSP00000352608.2:p.Phe4859=
ENST00000355481.8:c.14562C>T	ENSP00000347667.3:p.Phe4854=
ENST00000359596.7:c.14577C>T	ENSP00000352608.2:p.Phe4859=
ENST00000360985.7:c.14559C>T	ENSP00000354254.4:p.Phe4853=
NM_000540.2:c.14577C>T , LRG_766t1:c.14577C>T	NP_000531.2:p.Phe4859=
NM_001042723.1:c.14562C>T	NP_001036188.1:p.Phe4854=
XM_006723317.1:c.14559C>T	XP_006723380.1:p.Phe4853=
XM_006723319.1:c.14544C>T	XP_006723382.1:p.Phe4848=
XM_011527204.1:c.14574C>T	XP_011525506.1:p.Phe4858=
XM_011527205.1:c.14490C>T	XP_011525507.1:p.Phe4830=
XM_006723317.2:c.14559C>T	XP_006723380.1:p.Phe4853=
XM_006723319.2:c.14544C>T	XP_006723382.1:p.Phe4848=
XM_011527205.2:c.14490C>T	XP_011525507.1:p.Phe4830=
NM_000540.3:c.14577C>T MANE Select	NP_000531.2:p.Phe4859=
NM_001042723.2:c.14562C>T	NP_001036188.1:p.Phe4854=