Canonical Allele Identifier: CA405662495

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39034291G>C (hg19) ; chr19:g.38543651G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543651G>C , CM000681.2:g.38543651G>C	GRCh38
NC_000019.9:g.39034291G>C , CM000681.1:g.39034291G>C	GRCh37
NC_000019.8:g.43726131G>C	NCBI36
NG_008866.1:g.114952G>C , LRG_766:g.114952G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.308G>C
ENST00000689936.1:c.290G>C
ENST00000359596.8:c.11898G>C MANE Select	ENSP00000352608.2:p.Glu3966Asp
ENST00000355481.8:c.11883G>C	ENSP00000347667.3:p.Glu3961Asp
ENST00000359596.7:c.11898G>C	ENSP00000352608.2:p.Glu3966Asp
ENST00000360985.7:c.11880G>C	ENSP00000354254.4:p.Glu3960Asp
ENST00000593322.1:c.507G>C
ENST00000594335.5:c.5267G>C
NM_000540.2:c.11898G>C , LRG_766t1:c.11898G>C	NP_000531.2:p.Glu3966Asp
NM_001042723.1:c.11883G>C	NP_001036188.1:p.Glu3961Asp
XM_006723317.1:c.11880G>C	XP_006723380.1:p.Glu3960Asp
XM_006723319.1:c.11865G>C	XP_006723382.1:p.Glu3955Asp
XM_011527204.1:c.11895G>C	XP_011525506.1:p.Glu3965Asp
XM_011527205.1:c.11898G>C	XP_011525507.1:p.Glu3966Asp
XM_006723317.2:c.11880G>C	XP_006723380.1:p.Glu3960Asp
XM_006723319.2:c.11865G>C	XP_006723382.1:p.Glu3955Asp
XM_011527205.2:c.11898G>C	XP_011525507.1:p.Glu3966Asp
NM_000540.3:c.11898G>C MANE Select	NP_000531.2:p.Glu3966Asp
NM_001042723.2:c.11883G>C	NP_001036188.1:p.Glu3961Asp