Canonical Allele Identifier: CA2335088350

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572028T= , CM000681.2:g.38572028T=	GRCh38
NC_000019.9:g.39062668T= , CM000681.1:g.39062668T=	GRCh37
NC_000019.8:g.43754508T=	NCBI36
NG_008866.1:g.143329T= , LRG_766:g.143329T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.692T=
ENST00000688602.1:c.2089T=
ENST00000689936.1:c.2061T=
ENST00000359596.8:c.13756T= MANE Select	ENSP00000352608.2:p.Ser4586=
ENST00000355481.8:c.13741T=	ENSP00000347667.3:p.Ser4581=
ENST00000359596.7:c.13756T=	ENSP00000352608.2:p.Ser4586=
ENST00000360985.7:c.13738T=	ENSP00000354254.4:p.Ser4580=
ENST00000593677.1:c.216T=
NM_000540.2:c.13756T= , LRG_766t1:c.13756T=	NP_000531.2:p.Ser4586=
NM_001042723.1:c.13741T=	NP_001036188.1:p.Ser4581=
XM_006723317.1:c.13738T=	XP_006723380.1:p.Ser4580=
XM_006723319.1:c.13723T=	XP_006723382.1:p.Ser4575=
XM_011527204.1:c.13753T=	XP_011525506.1:p.Ser4585=
XM_011527205.1:c.13669T=	XP_011525507.1:p.Ser4557=
XM_006723317.2:c.13738T=	XP_006723380.1:p.Ser4580=
XM_006723319.2:c.13723T=	XP_006723382.1:p.Ser4575=
XM_011527205.2:c.13669T=	XP_011525507.1:p.Ser4557=
NM_000540.3:c.13756T= MANE Select	NP_000531.2:p.Ser4586=
NM_001042723.2:c.13741T=	NP_001036188.1:p.Ser4581=