Canonical Allele Identifier: CA061519

Gene: RYR1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38584993G>A , CM000681.2:g.38584993G>A	GRCh38
NC_000019.9:g.39075633G>A , CM000681.1:g.39075633G>A	GRCh37
NC_000019.8:g.43767473G>A	NCBI36
NG_008866.1:g.156294G>A , LRG_766:g.156294G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1633G>A
ENST00000688602.1:c.3030G>A
ENST00000689936.1:c.3002G>A
ENST00000692547.1:n.90G>A
ENST00000359596.8:c.14697G>A MANE Select	ENSP00000352608.2:p.Gly4899=
ENST00000355481.8:c.14682G>A	ENSP00000347667.3:p.Gly4894=
ENST00000359596.7:c.14697G>A	ENSP00000352608.2:p.Gly4899=
ENST00000360985.7:c.14679G>A	ENSP00000354254.4:p.Gly4893=
NM_000540.2:c.14697G>A , LRG_766t1:c.14697G>A	NP_000531.2:p.Gly4899=
NM_001042723.1:c.14682G>A	NP_001036188.1:p.Gly4894=
XM_006723317.1:c.14679G>A	XP_006723380.1:p.Gly4893=
XM_006723319.1:c.14664G>A	XP_006723382.1:p.Gly4888=
XM_011527204.1:c.14694G>A	XP_011525506.1:p.Gly4898=
XM_011527205.1:c.14610G>A	XP_011525507.1:p.Gly4870=
XM_006723317.2:c.14679G>A	XP_006723380.1:p.Gly4893=
XM_006723319.2:c.14664G>A	XP_006723382.1:p.Gly4888=
XM_011527205.2:c.14610G>A	XP_011525507.1:p.Gly4870=
NM_000540.3:c.14697G>A MANE Select	NP_000531.2:p.Gly4899=
NM_001042723.2:c.14682G>A	NP_001036188.1:p.Gly4894=