Canonical Allele Identifier: CA308109484

Gene: RYR1

Linked Data

• dbSNP Id: rs112906851
• MyVariant Identifiers: chr19:g.39056033C>G (hg19) ; chr19:g.38565393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565393C>G , CM000681.2:g.38565393C>G	GRCh38
NC_000019.9:g.39056033C>G , CM000681.1:g.39056033C>G	GRCh37
NC_000019.8:g.43747873C>G	NCBI36
NG_008866.1:g.136694C>G , LRG_766:g.136694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1469C>G
ENST00000689936.1:c.1451C>G
ENST00000359596.8:c.13059C>G MANE Select	ENSP00000352608.2:p.Gly4353=
ENST00000355481.8:c.13044C>G	ENSP00000347667.3:p.Gly4348=
ENST00000359596.7:c.13059C>G	ENSP00000352608.2:p.Gly4353=
ENST00000360985.7:c.13041C>G	ENSP00000354254.4:p.Gly4347=
NM_000540.2:c.13059C>G , LRG_766t1:c.13059C>G	NP_000531.2:p.Gly4353=
NM_001042723.1:c.13044C>G	NP_001036188.1:p.Gly4348=
XM_006723317.1:c.13041C>G	XP_006723380.1:p.Gly4347=
XM_006723319.1:c.13026C>G	XP_006723382.1:p.Gly4342=
XM_011527204.1:c.13056C>G	XP_011525506.1:p.Gly4352=
XM_011527205.1:c.13059C>G	XP_011525507.1:p.Gly4353=
XM_006723317.2:c.13041C>G	XP_006723380.1:p.Gly4347=
XM_006723319.2:c.13026C>G	XP_006723382.1:p.Gly4342=
XM_011527205.2:c.13059C>G	XP_011525507.1:p.Gly4353=
NM_000540.3:c.13059C>G MANE Select	NP_000531.2:p.Gly4353=
NM_001042723.2:c.13044C>G	NP_001036188.1:p.Gly4348=