Canonical Allele Identifier: CA2335074556

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543870G= , CM000681.2:g.38543870G=	GRCh38
NC_000019.9:g.39034510G= , CM000681.1:g.39034510G=	GRCh37
NC_000019.8:g.43726350G=	NCBI36
NG_008866.1:g.115171G= , LRG_766:g.115171G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.417G=
ENST00000689936.1:c.399G=
ENST00000359596.8:c.12007G= MANE Select	ENSP00000352608.2:p.Ala4003=
ENST00000355481.8:c.11992G=	ENSP00000347667.3:p.Ala3998=
ENST00000359596.7:c.12007G=	ENSP00000352608.2:p.Ala4003=
ENST00000360985.7:c.11989G=	ENSP00000354254.4:p.Ala3997=
ENST00000593322.1:c.616G=
ENST00000594335.5:c.5376G=
NM_000540.2:c.12007G= , LRG_766t1:c.12007G=	NP_000531.2:p.Ala4003=
NM_001042723.1:c.11992G=	NP_001036188.1:p.Ala3998=
XM_006723317.1:c.11989G=	XP_006723380.1:p.Ala3997=
XM_006723319.1:c.11974G=	XP_006723382.1:p.Ala3992=
XM_011527204.1:c.12004G=	XP_011525506.1:p.Ala4002=
XM_011527205.1:c.12007G=	XP_011525507.1:p.Ala4003=
XM_006723317.2:c.11989G=	XP_006723380.1:p.Ala3997=
XM_006723319.2:c.11974G=	XP_006723382.1:p.Ala3992=
XM_011527205.2:c.12007G=	XP_011525507.1:p.Ala4003=
NM_000540.3:c.12007G= MANE Select	NP_000531.2:p.Ala4003=
NM_001042723.2:c.11992G=	NP_001036188.1:p.Ala3998=