Canonical Allele Identifier: CA507355686

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565286-C-A
• MyVariant Identifiers: chr19:g.39055926C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565286C>A , CM000681.2:g.38565286C>A	GRCh38
NC_000019.9:g.39055926C>A , CM000681.1:g.39055926C>A	GRCh37
NC_000019.8:g.43747766C>A	NCBI36
NG_008866.1:g.136587C>A , LRG_766:g.136587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1362C>A
ENST00000689936.1:c.1344C>A
ENST00000359596.8:c.12952C>A MANE Select	ENSP00000352608.2:p.Arg4318=
ENST00000355481.8:c.12937C>A	ENSP00000347667.3:p.Arg4313=
ENST00000359596.7:c.12952C>A	ENSP00000352608.2:p.Arg4318=
ENST00000360985.7:c.12934C>A	ENSP00000354254.4:p.Arg4312=
NM_000540.2:c.12952C>A , LRG_766t1:c.12952C>A	NP_000531.2:p.Arg4318=
NM_001042723.1:c.12937C>A	NP_001036188.1:p.Arg4313=
XM_006723317.1:c.12934C>A	XP_006723380.1:p.Arg4312=
XM_006723319.1:c.12919C>A	XP_006723382.1:p.Arg4307=
XM_011527204.1:c.12949C>A	XP_011525506.1:p.Arg4317=
XM_011527205.1:c.12952C>A	XP_011525507.1:p.Arg4318=
XM_006723317.2:c.12934C>A	XP_006723380.1:p.Arg4312=
XM_006723319.2:c.12919C>A	XP_006723382.1:p.Arg4307=
XM_011527205.2:c.12952C>A	XP_011525507.1:p.Arg4318=
NM_000540.3:c.12952C>A MANE Select	NP_000531.2:p.Arg4318=
NM_001042723.2:c.12937C>A	NP_001036188.1:p.Arg4313=