Canonical Allele Identifier: CA2335065933

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38525455C= , CM000681.2:g.38525455C=	GRCh38
NC_000019.9:g.39016095C= , CM000681.1:g.39016095C=	GRCh37
NC_000019.8:g.43707935C=	NCBI36
NG_008866.1:g.96756C= , LRG_766:g.96756C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.10579C= MANE Select	NP_000531.2:p.Pro3527=
ENST00000359596.8:c.10579C= MANE Select	ENSP00000352608.2:p.Pro3527=
NM_000540.2:c.10579C= , LRG_766t1:c.10579C=	NP_000531.2:p.Pro3527=
NM_001042723.1:c.10564C=	NP_001036188.1:p.Pro3522=
NM_001042723.2:c.10564C=	NP_001036188.1:p.Pro3522=
ENST00000355481.8:c.10564C=	ENSP00000347667.3:p.Pro3522=
ENST00000359596.7:c.10579C=	ENSP00000352608.2:p.Pro3527=
ENST00000360985.7:c.10561C=	ENSP00000354254.4:p.Pro3521=
ENST00000594335.5:c.3966C=
ENST00000599547.5:c.1386C=
ENST00000599547.6:c.10518C=	ENSP00000471601.2:n.10518C=
XM_006723317.1:c.10579C=	XP_006723380.1:p.Pro3527=
XM_006723317.2:c.10579C=	XP_006723380.1:p.Pro3527=
XM_006723319.1:c.10564C=	XP_006723382.1:p.Pro3522=
XM_006723319.2:c.10564C=	XP_006723382.1:p.Pro3522=
XM_011527204.1:c.10576C=	XP_011525506.1:p.Pro3526=
XM_011527205.1:c.10579C=	XP_011525507.1:p.Pro3527=
XM_011527205.2:c.10579C=	XP_011525507.1:p.Pro3527=