Canonical Allele Identifier: CA507355779

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565348-A-G
• MyVariant Identifiers: chr19:g.39055988A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565348A>G , CM000681.2:g.38565348A>G	GRCh38
NC_000019.9:g.39055988A>G , CM000681.1:g.39055988A>G	GRCh37
NC_000019.8:g.43747828A>G	NCBI36
NG_008866.1:g.136649A>G , LRG_766:g.136649A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1424A>G
ENST00000689936.1:c.1406A>G
ENST00000359596.8:c.13014A>G MANE Select	ENSP00000352608.2:p.Ala4338=
ENST00000355481.8:c.12999A>G	ENSP00000347667.3:p.Ala4333=
ENST00000359596.7:c.13014A>G	ENSP00000352608.2:p.Ala4338=
ENST00000360985.7:c.12996A>G	ENSP00000354254.4:p.Ala4332=
NM_000540.2:c.13014A>G , LRG_766t1:c.13014A>G	NP_000531.2:p.Ala4338=
NM_001042723.1:c.12999A>G	NP_001036188.1:p.Ala4333=
XM_006723317.1:c.12996A>G	XP_006723380.1:p.Ala4332=
XM_006723319.1:c.12981A>G	XP_006723382.1:p.Ala4327=
XM_011527204.1:c.13011A>G	XP_011525506.1:p.Ala4337=
XM_011527205.1:c.13014A>G	XP_011525507.1:p.Ala4338=
XM_006723317.2:c.12996A>G	XP_006723380.1:p.Ala4332=
XM_006723319.2:c.12981A>G	XP_006723382.1:p.Ala4327=
XM_011527205.2:c.13014A>G	XP_011525507.1:p.Ala4338=
NM_000540.3:c.13014A>G MANE Select	NP_000531.2:p.Ala4338=
NM_001042723.2:c.12999A>G	NP_001036188.1:p.Ala4333=