Canonical Allele Identifier: CA405672668

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565272-T-C
• MyVariant Identifiers: chr19:g.39055912T>C (hg19) ; chr19:g.38565272T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565272T>C , CM000681.2:g.38565272T>C	GRCh38
NC_000019.9:g.39055912T>C , CM000681.1:g.39055912T>C	GRCh37
NC_000019.8:g.43747752T>C	NCBI36
NG_008866.1:g.136573T>C , LRG_766:g.136573T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1348T>C
ENST00000689936.1:c.1330T>C
ENST00000359596.8:c.12938T>C MANE Select	ENSP00000352608.2:p.Leu4313Pro
ENST00000355481.8:c.12923T>C	ENSP00000347667.3:p.Leu4308Pro
ENST00000359596.7:c.12938T>C	ENSP00000352608.2:p.Leu4313Pro
ENST00000360985.7:c.12920T>C	ENSP00000354254.4:p.Leu4307Pro
NM_000540.2:c.12938T>C , LRG_766t1:c.12938T>C	NP_000531.2:p.Leu4313Pro
NM_001042723.1:c.12923T>C	NP_001036188.1:p.Leu4308Pro
XM_006723317.1:c.12920T>C	XP_006723380.1:p.Leu4307Pro
XM_006723319.1:c.12905T>C	XP_006723382.1:p.Leu4302Pro
XM_011527204.1:c.12935T>C	XP_011525506.1:p.Leu4312Pro
XM_011527205.1:c.12938T>C	XP_011525507.1:p.Leu4313Pro
XM_006723317.2:c.12920T>C	XP_006723380.1:p.Leu4307Pro
XM_006723319.2:c.12905T>C	XP_006723382.1:p.Leu4302Pro
XM_011527205.2:c.12938T>C	XP_011525507.1:p.Leu4313Pro
NM_000540.3:c.12938T>C MANE Select	NP_000531.2:p.Leu4313Pro
NM_001042723.2:c.12923T>C	NP_001036188.1:p.Leu4308Pro