Canonical Allele Identifier: CA507355599

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565432-C-G
• MyVariant Identifiers: chr19:g.39056072C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565432C>G , CM000681.2:g.38565432C>G	GRCh38
NC_000019.9:g.39056072C>G , CM000681.1:g.39056072C>G	GRCh37
NC_000019.8:g.43747912C>G	NCBI36
NG_008866.1:g.136733C>G , LRG_766:g.136733C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.34C>G
ENST00000688602.1:c.1508C>G
ENST00000689936.1:c.1490C>G
ENST00000359596.8:c.13098C>G MANE Select	ENSP00000352608.2:p.Gly4366=
ENST00000355481.8:c.13083C>G	ENSP00000347667.3:p.Gly4361=
ENST00000359596.7:c.13098C>G	ENSP00000352608.2:p.Gly4366=
ENST00000360985.7:c.13080C>G	ENSP00000354254.4:p.Gly4360=
NM_000540.2:c.13098C>G , LRG_766t1:c.13098C>G	NP_000531.2:p.Gly4366=
NM_001042723.1:c.13083C>G	NP_001036188.1:p.Gly4361=
XM_006723317.1:c.13080C>G	XP_006723380.1:p.Gly4360=
XM_006723319.1:c.13065C>G	XP_006723382.1:p.Gly4355=
XM_011527204.1:c.13095C>G	XP_011525506.1:p.Gly4365=
XM_011527205.1:c.13098C>G	XP_011525507.1:p.Gly4366=
XM_006723317.2:c.13080C>G	XP_006723380.1:p.Gly4360=
XM_006723319.2:c.13065C>G	XP_006723382.1:p.Gly4355=
XM_011527205.2:c.13098C>G	XP_011525507.1:p.Gly4366=
NM_000540.3:c.13098C>G MANE Select	NP_000531.2:p.Gly4366=
NM_001042723.2:c.13083C>G	NP_001036188.1:p.Gly4361=