Canonical Allele Identifier: CA507236861

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38527022T>C , CM000681.2:g.38527022T>C	GRCh38
NC_000019.9:g.39017662T>C , CM000681.1:g.39017662T>C	GRCh37
NC_000019.8:g.43709502T>C	NCBI36
NG_008866.1:g.98323T>C , LRG_766:g.98323T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.10656T>C MANE Select	NP_000531.2:p.Phe3552=
ENST00000359596.8:c.10656T>C MANE Select	ENSP00000352608.2:p.Phe3552=
NM_000540.2:c.10656T>C , LRG_766t1:c.10656T>C	NP_000531.2:p.Phe3552=
NM_001042723.1:c.10641T>C	NP_001036188.1:p.Phe3547=
NM_001042723.2:c.10641T>C	NP_001036188.1:p.Phe3547=
ENST00000355481.8:c.10641T>C	ENSP00000347667.3:p.Phe3547=
ENST00000359596.7:c.10656T>C	ENSP00000352608.2:p.Phe3552=
ENST00000360985.7:c.10638T>C	ENSP00000354254.4:p.Phe3546=
ENST00000594335.5:c.4043T>C
ENST00000599547.5:c.1463T>C
ENST00000599547.6:c.10595T>C	ENSP00000471601.2:n.10595T>C
XM_006723317.1:c.10656T>C	XP_006723380.1:p.Phe3552=
XM_006723317.2:c.10656T>C	XP_006723380.1:p.Phe3552=
XM_006723319.1:c.10641T>C	XP_006723382.1:p.Phe3547=
XM_006723319.2:c.10641T>C	XP_006723382.1:p.Phe3547=
XM_011527204.1:c.10653T>C	XP_011525506.1:p.Phe3551=
XM_011527205.1:c.10656T>C	XP_011525507.1:p.Phe3552=
XM_011527205.2:c.10656T>C	XP_011525507.1:p.Phe3552=
XR_001753936.1:n.502A>G