Canonical Allele Identifier: CA507355439

Gene: RYR1

Linked Data

• dbSNP Id: rs1184700540
• MyVariant Identifiers: chr19:g.39055820C>G (hg19) ; chr19:g.38565180C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565180C>G , CM000681.2:g.38565180C>G	GRCh38
NC_000019.9:g.39055820C>G , CM000681.1:g.39055820C>G	GRCh37
NC_000019.8:g.43747660C>G	NCBI36
NG_008866.1:g.136481C>G , LRG_766:g.136481C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1256C>G
ENST00000689936.1:c.1238C>G
ENST00000359596.8:c.12846C>G MANE Select	ENSP00000352608.2:p.Leu4282=
ENST00000355481.8:c.12831C>G	ENSP00000347667.3:p.Leu4277=
ENST00000359596.7:c.12846C>G	ENSP00000352608.2:p.Leu4282=
ENST00000360985.7:c.12828C>G	ENSP00000354254.4:p.Leu4276=
ENST00000594335.5:c.6215C>G
NM_000540.2:c.12846C>G , LRG_766t1:c.12846C>G	NP_000531.2:p.Leu4282=
NM_001042723.1:c.12831C>G	NP_001036188.1:p.Leu4277=
XM_006723317.1:c.12828C>G	XP_006723380.1:p.Leu4276=
XM_006723319.1:c.12813C>G	XP_006723382.1:p.Leu4271=
XM_011527204.1:c.12843C>G	XP_011525506.1:p.Leu4281=
XM_011527205.1:c.12846C>G	XP_011525507.1:p.Leu4282=
XM_006723317.2:c.12828C>G	XP_006723380.1:p.Leu4276=
XM_006723319.2:c.12813C>G	XP_006723382.1:p.Leu4271=
XM_011527205.2:c.12846C>G	XP_011525507.1:p.Leu4282=
NM_000540.3:c.12846C>G MANE Select	NP_000531.2:p.Leu4282=
NM_001042723.2:c.12831C>G	NP_001036188.1:p.Leu4277=