Canonical Allele Identifier: CA308109167

Gene: RYR1

Linked Data

• dbSNP Id: rs949615251
• gnomAD v4: 19-38565125-G-T
• MyVariant Identifiers: chr19:g.39055765G>T (hg19) ; chr19:g.38565125G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565125G>T , CM000681.2:g.38565125G>T	GRCh38
NC_000019.9:g.39055765G>T , CM000681.1:g.39055765G>T	GRCh37
NC_000019.8:g.43747605G>T	NCBI36
NG_008866.1:g.136426G>T , LRG_766:g.136426G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.1201G>T
ENST00000689936.1:c.1183G>T
ENST00000359596.8:c.12791G>T MANE Select	ENSP00000352608.2:p.Gly4264Val
ENST00000355481.8:c.12776G>T	ENSP00000347667.3:p.Gly4259Val
ENST00000359596.7:c.12791G>T	ENSP00000352608.2:p.Gly4264Val
ENST00000360985.7:c.12773G>T	ENSP00000354254.4:p.Gly4258Val
ENST00000594335.5:c.6160G>T
NM_000540.2:c.12791G>T , LRG_766t1:c.12791G>T	NP_000531.2:p.Gly4264Val
NM_001042723.1:c.12776G>T	NP_001036188.1:p.Gly4259Val
XM_006723317.1:c.12773G>T	XP_006723380.1:p.Gly4258Val
XM_006723319.1:c.12758G>T	XP_006723382.1:p.Gly4253Val
XM_011527204.1:c.12788G>T	XP_011525506.1:p.Gly4263Val
XM_011527205.1:c.12791G>T	XP_011525507.1:p.Gly4264Val
XM_006723317.2:c.12773G>T	XP_006723380.1:p.Gly4258Val
XM_006723319.2:c.12758G>T	XP_006723382.1:p.Gly4253Val
XM_011527205.2:c.12791G>T	XP_011525507.1:p.Gly4264Val
NM_000540.3:c.12791G>T MANE Select	NP_000531.2:p.Gly4264Val
NM_001042723.2:c.12776G>T	NP_001036188.1:p.Gly4259Val