Canonical Allele Identifier: CA2335051173

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38496301T= , CM000681.2:g.38496301T=	GRCh38
NC_000019.9:g.38986941T= , CM000681.1:g.38986941T=	GRCh37
NC_000019.8:g.43678781T=	NCBI36
NG_008866.1:g.67602T= , LRG_766:g.67602T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.6635T=	ENSP00000471601.2:p.Val2212=
ENST00000359596.8:c.6635T= MANE Select	ENSP00000352608.2:p.Val2212=
ENST00000355481.8:c.6635T=	ENSP00000347667.3:p.Val2212=
ENST00000359596.7:c.6635T=	ENSP00000352608.2:p.Val2212=
ENST00000360985.7:c.6632T=	ENSP00000354254.4:p.Val2211=
ENST00000594335.5:c.87T=
NM_000540.2:c.6635T= , LRG_766t1:c.6635T=	NP_000531.2:p.Val2212=
NM_001042723.1:c.6635T=	NP_001036188.1:p.Val2212=
XM_006723317.1:c.6635T=	XP_006723380.1:p.Val2212=
XM_006723319.1:c.6635T=	XP_006723382.1:p.Val2212=
XM_011527204.1:c.6632T=	XP_011525506.1:p.Val2211=
XM_011527205.1:c.6635T=	XP_011525507.1:p.Val2212=
XM_006723317.2:c.6635T=	XP_006723380.1:p.Val2212=
XM_006723319.2:c.6635T=	XP_006723382.1:p.Val2212=
XM_011527205.2:c.6635T=	XP_011525507.1:p.Val2212=
XR_001753735.1:n.6718T=
NM_000540.3:c.6635T= MANE Select	NP_000531.2:p.Val2212=
NM_001042723.2:c.6635T=	NP_001036188.1:p.Val2212=