Canonical Allele Identifier: CA2335053468

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38500855C= , CM000681.2:g.38500855C=	GRCh38
NC_000019.9:g.38991495C= , CM000681.1:g.38991495C=	GRCh37
NC_000019.8:g.43683335C=	NCBI36
NG_008866.1:g.72156C= , LRG_766:g.72156C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7479C=	ENSP00000471601.2:p.Ser2493=
ENST00000359596.8:c.7479C= MANE Select	ENSP00000352608.2:p.Ser2493=
ENST00000355481.8:c.7479C=	ENSP00000347667.3:p.Ser2493=
ENST00000359596.7:c.7479C=	ENSP00000352608.2:p.Ser2493=
ENST00000360985.7:c.7476C=	ENSP00000354254.4:p.Ser2492=
ENST00000594335.5:c.931C=
NM_000540.2:c.7479C= , LRG_766t1:c.7479C=	NP_000531.2:p.Ser2493=
NM_001042723.1:c.7479C=	NP_001036188.1:p.Ser2493=
XM_006723317.1:c.7479C=	XP_006723380.1:p.Ser2493=
XM_006723319.1:c.7479C=	XP_006723382.1:p.Ser2493=
XM_011527204.1:c.7476C=	XP_011525506.1:p.Ser2492=
XM_011527205.1:c.7479C=	XP_011525507.1:p.Ser2493=
XM_006723317.2:c.7479C=	XP_006723380.1:p.Ser2493=
XM_006723319.2:c.7479C=	XP_006723382.1:p.Ser2493=
XM_011527205.2:c.7479C=	XP_011525507.1:p.Ser2493=
XR_001753735.1:n.7562C=
NM_000540.3:c.7479C= MANE Select	NP_000531.2:p.Ser2493=
NM_001042723.2:c.7479C=	NP_001036188.1:p.Ser2493=