Canonical Allele Identifier: CA2335092255

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580004A= , CM000681.2:g.38580004A=	GRCh38
NC_000019.9:g.39070644A= , CM000681.1:g.39070644A=	GRCh37
NC_000019.8:g.43762484A=	NCBI36
NG_008866.1:g.151305A= , LRG_766:g.151305A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.14387A= MANE Select	NP_000531.2:p.Tyr4796=
ENST00000359596.8:c.14387A= MANE Select	ENSP00000352608.2:p.Tyr4796=
NM_000540.2:c.14387A= , LRG_766t1:c.14387A=	NP_000531.2:p.Tyr4796=
NM_001042723.1:c.14372A=	NP_001036188.1:p.Tyr4791=
NM_001042723.2:c.14372A=	NP_001036188.1:p.Tyr4791=
ENST00000355481.8:c.14372A=	ENSP00000347667.3:p.Tyr4791=
ENST00000359596.7:c.14387A=	ENSP00000352608.2:p.Tyr4796=
ENST00000360985.7:c.14369A=	ENSP00000354254.4:p.Tyr4790=
ENST00000593677.2:c.1323A=
ENST00000688602.1:c.2720A=
ENST00000689936.1:c.2692A=
XM_006723317.1:c.14369A=	XP_006723380.1:p.Tyr4790=
XM_006723317.2:c.14369A=	XP_006723380.1:p.Tyr4790=
XM_006723319.1:c.14354A=	XP_006723382.1:p.Tyr4785=
XM_006723319.2:c.14354A=	XP_006723382.1:p.Tyr4785=
XM_011527204.1:c.14384A=	XP_011525506.1:p.Tyr4795=
XM_011527205.1:c.14300A=	XP_011525507.1:p.Tyr4767=
XM_011527205.2:c.14300A=	XP_011525507.1:p.Tyr4767=