Canonical Allele Identifier: CA405674178

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565526-G-C
• MyVariant Identifiers: chr19:g.39056166G>C (hg19) ; chr19:g.38565526G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565526G>C , CM000681.2:g.38565526G>C	GRCh38
NC_000019.9:g.39056166G>C , CM000681.1:g.39056166G>C	GRCh37
NC_000019.8:g.43748006G>C	NCBI36
NG_008866.1:g.136827G>C , LRG_766:g.136827G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.128G>C
ENST00000688602.1:c.1602G>C
ENST00000689936.1:c.1584G>C
ENST00000359596.8:c.13192G>C MANE Select	ENSP00000352608.2:p.Gly4398Arg
ENST00000355481.8:c.13177G>C	ENSP00000347667.3:p.Gly4393Arg
ENST00000359596.7:c.13192G>C	ENSP00000352608.2:p.Gly4398Arg
ENST00000360985.7:c.13174G>C	ENSP00000354254.4:p.Gly4392Arg
NM_000540.2:c.13192G>C , LRG_766t1:c.13192G>C	NP_000531.2:p.Gly4398Arg
NM_001042723.1:c.13177G>C	NP_001036188.1:p.Gly4393Arg
XM_006723317.1:c.13174G>C	XP_006723380.1:p.Gly4392Arg
XM_006723319.1:c.13159G>C	XP_006723382.1:p.Gly4387Arg
XM_011527204.1:c.13189G>C	XP_011525506.1:p.Gly4397Arg
XM_011527205.1:c.13192G>C	XP_011525507.1:p.Gly4398Arg
XM_006723317.2:c.13174G>C	XP_006723380.1:p.Gly4392Arg
XM_006723319.2:c.13159G>C	XP_006723382.1:p.Gly4387Arg
XM_011527205.2:c.13192G>C	XP_011525507.1:p.Gly4398Arg
NM_000540.3:c.13192G>C MANE Select	NP_000531.2:p.Gly4398Arg
NM_001042723.2:c.13177G>C	NP_001036188.1:p.Gly4393Arg