Canonical Allele Identifier: CA405662572

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39034300G>T (hg19) ; chr19:g.38543660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543660G>T , CM000681.2:g.38543660G>T	GRCh38
NC_000019.9:g.39034300G>T , CM000681.1:g.39034300G>T	GRCh37
NC_000019.8:g.43726140G>T	NCBI36
NG_008866.1:g.114961G>T , LRG_766:g.114961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.317G>T
ENST00000689936.1:c.299G>T
ENST00000359596.8:c.11907G>T MANE Select	ENSP00000352608.2:p.Gln3969His
ENST00000355481.8:c.11892G>T	ENSP00000347667.3:p.Gln3964His
ENST00000359596.7:c.11907G>T	ENSP00000352608.2:p.Gln3969His
ENST00000360985.7:c.11889G>T	ENSP00000354254.4:p.Gln3963His
ENST00000593322.1:c.516G>T
ENST00000594335.5:c.5276G>T
NM_000540.2:c.11907G>T , LRG_766t1:c.11907G>T	NP_000531.2:p.Gln3969His
NM_001042723.1:c.11892G>T	NP_001036188.1:p.Gln3964His
XM_006723317.1:c.11889G>T	XP_006723380.1:p.Gln3963His
XM_006723319.1:c.11874G>T	XP_006723382.1:p.Gln3958His
XM_011527204.1:c.11904G>T	XP_011525506.1:p.Gln3968His
XM_011527205.1:c.11907G>T	XP_011525507.1:p.Gln3969His
XM_006723317.2:c.11889G>T	XP_006723380.1:p.Gln3963His
XM_006723319.2:c.11874G>T	XP_006723382.1:p.Gln3958His
XM_011527205.2:c.11907G>T	XP_011525507.1:p.Gln3969His
NM_000540.3:c.11907G>T MANE Select	NP_000531.2:p.Gln3969His
NM_001042723.2:c.11892G>T	NP_001036188.1:p.Gln3964His