Canonical Allele Identifier: CA632867465

Gene: RYR1

Linked Data

• dbSNP Id: rs1464714333
• gnomAD v2: 19-39026628-T-C
• gnomAD v4: 19-38535988-T-C
• MyVariant Identifiers: chr19:g.39026628T>C (hg19) ; chr19:g.38535988T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38535988T>C , CM000681.2:g.38535988T>C	GRCh38
NC_000019.9:g.39026628T>C , CM000681.1:g.39026628T>C	GRCh37
NC_000019.8:g.43718468T>C	NCBI36
NG_008866.1:g.107289T>C , LRG_766:g.107289T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359596.8:c.11517-9T>C MANE Select	ENSP00000352608.2:n.11517-9T>C
ENST00000355481.8:c.11502-9T>C	ENSP00000347667.3:n.11502-9T>C
ENST00000359596.7:c.11517-9T>C	ENSP00000352608.2:n.11517-9T>C
ENST00000360985.7:c.11499-9T>C	ENSP00000354254.4:n.11499-9T>C
ENST00000593322.1:c.217+596T>C
ENST00000594335.5:c.4904-9T>C
ENST00000596431.5:c.246-9T>C	ENSP00000470848.1:n.246-9T>C
ENST00000601514.5:c.798-9T>C	ENSP00000472497.1:n.798-9T>C
NM_000540.2:c.11517-9T>C , LRG_766t1:c.11517-9T>C	NP_000531.2:n.11517-9T>C
NM_001042723.1:c.11502-9T>C	NP_001036188.1:n.11502-9T>C
XM_006723317.1:c.11517-9T>C	XP_006723380.1:n.11517-9T>C
XM_006723319.1:c.11502-9T>C	XP_006723382.1:n.11502-9T>C
XM_011527204.1:c.11514-9T>C	XP_011525506.1:n.11514-9T>C
XM_011527205.1:c.11517-9T>C	XP_011525507.1:n.11517-9T>C
XM_006723317.2:c.11517-9T>C	XP_006723380.1:n.11517-9T>C
XM_006723319.2:c.11502-9T>C	XP_006723382.1:n.11502-9T>C
XM_011527205.2:c.11517-9T>C	XP_011525507.1:n.11517-9T>C
NM_000540.3:c.11517-9T>C MANE Select	NP_000531.2:n.11517-9T>C
NM_001042723.2:c.11502-9T>C	NP_001036188.1:n.11502-9T>C