Canonical Allele Identifier: CA405672575

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565253-G-C
• MyVariant Identifiers: chr19:g.39055893G>C (hg19) ; chr19:g.38565253G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565253G>C , CM000681.2:g.38565253G>C	GRCh38
NC_000019.9:g.39055893G>C , CM000681.1:g.39055893G>C	GRCh37
NC_000019.8:g.43747733G>C	NCBI36
NG_008866.1:g.136554G>C , LRG_766:g.136554G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1329G>C
ENST00000689936.1:c.1311G>C
ENST00000359596.8:c.12919G>C MANE Select	ENSP00000352608.2:p.Gly4307Arg
ENST00000355481.8:c.12904G>C	ENSP00000347667.3:p.Gly4302Arg
ENST00000359596.7:c.12919G>C	ENSP00000352608.2:p.Gly4307Arg
ENST00000360985.7:c.12901G>C	ENSP00000354254.4:p.Gly4301Arg
NM_000540.2:c.12919G>C , LRG_766t1:c.12919G>C	NP_000531.2:p.Gly4307Arg
NM_001042723.1:c.12904G>C	NP_001036188.1:p.Gly4302Arg
XM_006723317.1:c.12901G>C	XP_006723380.1:p.Gly4301Arg
XM_006723319.1:c.12886G>C	XP_006723382.1:p.Gly4296Arg
XM_011527204.1:c.12916G>C	XP_011525506.1:p.Gly4306Arg
XM_011527205.1:c.12919G>C	XP_011525507.1:p.Gly4307Arg
XM_006723317.2:c.12901G>C	XP_006723380.1:p.Gly4301Arg
XM_006723319.2:c.12886G>C	XP_006723382.1:p.Gly4296Arg
XM_011527205.2:c.12919G>C	XP_011525507.1:p.Gly4307Arg
NM_000540.3:c.12919G>C MANE Select	NP_000531.2:p.Gly4307Arg
NM_001042723.2:c.12904G>C	NP_001036188.1:p.Gly4302Arg