Canonical Allele Identifier: CA2335092310

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580122G= , CM000681.2:g.38580122G=	GRCh38
NC_000019.9:g.39070762G= , CM000681.1:g.39070762G=	GRCh37
NC_000019.8:g.43762602G=	NCBI36
NG_008866.1:g.151423G= , LRG_766:g.151423G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1441G=
ENST00000688602.1:c.2838G=
ENST00000689936.1:c.2810G=
ENST00000359596.8:c.14505G= MANE Select	ENSP00000352608.2:p.Gly4835=
ENST00000355481.8:c.14490G=	ENSP00000347667.3:p.Gly4830=
ENST00000359596.7:c.14505G=	ENSP00000352608.2:p.Gly4835=
ENST00000360985.7:c.14487G=	ENSP00000354254.4:p.Gly4829=
NM_000540.2:c.14505G= , LRG_766t1:c.14505G=	NP_000531.2:p.Gly4835=
NM_001042723.1:c.14490G=	NP_001036188.1:p.Gly4830=
XM_006723317.1:c.14487G=	XP_006723380.1:p.Gly4829=
XM_006723319.1:c.14472G=	XP_006723382.1:p.Gly4824=
XM_011527204.1:c.14502G=	XP_011525506.1:p.Gly4834=
XM_011527205.1:c.14418G=	XP_011525507.1:p.Gly4806=
XM_006723317.2:c.14487G=	XP_006723380.1:p.Gly4829=
XM_006723319.2:c.14472G=	XP_006723382.1:p.Gly4824=
XM_011527205.2:c.14418G=	XP_011525507.1:p.Gly4806=
NM_000540.3:c.14505G= MANE Select	NP_000531.2:p.Gly4835=
NM_001042723.2:c.14490G=	NP_001036188.1:p.Gly4830=