Canonical Allele Identifier: CA2584910053

Gene: RYR1

Linked Data

• gnomAD v4: 19-38572290-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572290T>C , CM000681.2:g.38572290T>C	GRCh38
NC_000019.9:g.39062930T>C , CM000681.1:g.39062930T>C	GRCh37
NC_000019.8:g.43754770T>C	NCBI36
NG_008866.1:g.143591T>C , LRG_766:g.143591T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.934+20T>C
ENST00000688602.1:c.2331+20T>C
ENST00000689936.1:c.2303+20T>C
ENST00000359596.8:c.13998+20T>C MANE Select	ENSP00000352608.2:n.13998+20T>C
ENST00000355481.8:c.13983+20T>C	ENSP00000347667.3:n.13983+20T>C
ENST00000359596.7:c.13998+20T>C	ENSP00000352608.2:n.13998+20T>C
ENST00000360985.7:c.13980+20T>C	ENSP00000354254.4:n.13980+20T>C
NM_000540.2:c.13998+20T>C , LRG_766t1:c.13998+20T>C	NP_000531.2:n.13998+20T>C
NM_001042723.1:c.13983+20T>C	NP_001036188.1:n.13983+20T>C
XM_006723317.1:c.13980+20T>C	XP_006723380.1:n.13980+20T>C
XM_006723319.1:c.13965+20T>C	XP_006723382.1:n.13965+20T>C
XM_011527204.1:c.13995+20T>C	XP_011525506.1:n.13995+20T>C
XM_011527205.1:c.13911+20T>C	XP_011525507.1:n.13911+20T>C
XM_006723317.2:c.13980+20T>C	XP_006723380.1:n.13980+20T>C
XM_006723319.2:c.13965+20T>C	XP_006723382.1:n.13965+20T>C
XM_011527205.2:c.13911+20T>C	XP_011525507.1:n.13911+20T>C
NM_000540.3:c.13998+20T>C MANE Select	NP_000531.2:n.13998+20T>C
NM_001042723.2:c.13983+20T>C	NP_001036188.1:n.13983+20T>C