Canonical Allele Identifier: CA405656359

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39026636G>T (hg19) ; chr19:g.38535996G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38535996G>T , CM000681.2:g.38535996G>T	GRCh38
NC_000019.9:g.39026636G>T , CM000681.1:g.39026636G>T	GRCh37
NC_000019.8:g.43718476G>T	NCBI36
NG_008866.1:g.107297G>T , LRG_766:g.107297G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359596.8:c.11517-1G>T MANE Select	ENSP00000352608.2:n.11517-1G>T
ENST00000355481.8:c.11502-1G>T	ENSP00000347667.3:n.11502-1G>T
ENST00000359596.7:c.11517-1G>T	ENSP00000352608.2:n.11517-1G>T
ENST00000360985.7:c.11499-1G>T	ENSP00000354254.4:n.11499-1G>T
ENST00000593322.1:c.217+604G>T
ENST00000594335.5:c.4904-1G>T
ENST00000596431.5:c.246-1G>T	ENSP00000470848.1:n.246-1G>T
ENST00000601514.5:c.798-1G>T	ENSP00000472497.1:n.798-1G>T
NM_000540.2:c.11517-1G>T , LRG_766t1:c.11517-1G>T	NP_000531.2:n.11517-1G>T
NM_001042723.1:c.11502-1G>T	NP_001036188.1:n.11502-1G>T
XM_006723317.1:c.11517-1G>T	XP_006723380.1:n.11517-1G>T
XM_006723319.1:c.11502-1G>T	XP_006723382.1:n.11502-1G>T
XM_011527204.1:c.11514-1G>T	XP_011525506.1:n.11514-1G>T
XM_011527205.1:c.11517-1G>T	XP_011525507.1:n.11517-1G>T
XM_006723317.2:c.11517-1G>T	XP_006723380.1:n.11517-1G>T
XM_006723319.2:c.11502-1G>T	XP_006723382.1:n.11502-1G>T
XM_011527205.2:c.11517-1G>T	XP_011525507.1:n.11517-1G>T
NM_000540.3:c.11517-1G>T MANE Select	NP_000531.2:n.11517-1G>T
NM_001042723.2:c.11502-1G>T	NP_001036188.1:n.11502-1G>T