Canonical Allele Identifier: CA405662328

Gene: RYR1

Linked Data

• gnomAD v4: 19-38543635-T-G
• MyVariant Identifiers: chr19:g.39034275T>G (hg19) ; chr19:g.38543635T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543635T>G , CM000681.2:g.38543635T>G	GRCh38
NC_000019.9:g.39034275T>G , CM000681.1:g.39034275T>G	GRCh37
NC_000019.8:g.43726115T>G	NCBI36
NG_008866.1:g.114936T>G , LRG_766:g.114936T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.292T>G
ENST00000689936.1:c.274T>G
ENST00000359596.8:c.11882T>G MANE Select	ENSP00000352608.2:p.Phe3961Cys
ENST00000355481.8:c.11867T>G	ENSP00000347667.3:p.Phe3956Cys
ENST00000359596.7:c.11882T>G	ENSP00000352608.2:p.Phe3961Cys
ENST00000360985.7:c.11864T>G	ENSP00000354254.4:p.Phe3955Cys
ENST00000593322.1:c.491T>G
ENST00000594335.5:c.5251T>G
NM_000540.2:c.11882T>G , LRG_766t1:c.11882T>G	NP_000531.2:p.Phe3961Cys
NM_001042723.1:c.11867T>G	NP_001036188.1:p.Phe3956Cys
XM_006723317.1:c.11864T>G	XP_006723380.1:p.Phe3955Cys
XM_006723319.1:c.11849T>G	XP_006723382.1:p.Phe3950Cys
XM_011527204.1:c.11879T>G	XP_011525506.1:p.Phe3960Cys
XM_011527205.1:c.11882T>G	XP_011525507.1:p.Phe3961Cys
XM_006723317.2:c.11864T>G	XP_006723380.1:p.Phe3955Cys
XM_006723319.2:c.11849T>G	XP_006723382.1:p.Phe3950Cys
XM_011527205.2:c.11882T>G	XP_011525507.1:p.Phe3961Cys
NM_000540.3:c.11882T>G MANE Select	NP_000531.2:p.Phe3961Cys
NM_001042723.2:c.11867T>G	NP_001036188.1:p.Phe3956Cys