Canonical Allele Identifier: CA507242721

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39034509C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543869C>G , CM000681.2:g.38543869C>G	GRCh38
NC_000019.9:g.39034509C>G , CM000681.1:g.39034509C>G	GRCh37
NC_000019.8:g.43726349C>G	NCBI36
NG_008866.1:g.115170C>G , LRG_766:g.115170C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.416C>G
ENST00000689936.1:c.398C>G
ENST00000359596.8:c.12006C>G MANE Select	ENSP00000352608.2:p.Leu4002=
ENST00000355481.8:c.11991C>G	ENSP00000347667.3:p.Leu3997=
ENST00000359596.7:c.12006C>G	ENSP00000352608.2:p.Leu4002=
ENST00000360985.7:c.11988C>G	ENSP00000354254.4:p.Leu3996=
ENST00000593322.1:c.615C>G
ENST00000594335.5:c.5375C>G
NM_000540.2:c.12006C>G , LRG_766t1:c.12006C>G	NP_000531.2:p.Leu4002=
NM_001042723.1:c.11991C>G	NP_001036188.1:p.Leu3997=
XM_006723317.1:c.11988C>G	XP_006723380.1:p.Leu3996=
XM_006723319.1:c.11973C>G	XP_006723382.1:p.Leu3991=
XM_011527204.1:c.12003C>G	XP_011525506.1:p.Leu4001=
XM_011527205.1:c.12006C>G	XP_011525507.1:p.Leu4002=
XM_006723317.2:c.11988C>G	XP_006723380.1:p.Leu3996=
XM_006723319.2:c.11973C>G	XP_006723382.1:p.Leu3991=
XM_011527205.2:c.12006C>G	XP_011525507.1:p.Leu4002=
NM_000540.3:c.12006C>G MANE Select	NP_000531.2:p.Leu4002=
NM_001042723.2:c.11991C>G	NP_001036188.1:p.Leu3997=