Canonical Allele Identifier: CA405687603

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071026G>A (hg19) ; chr19:g.38580386G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580386G>A , CM000681.2:g.38580386G>A	GRCh38
NC_000019.9:g.39071026G>A , CM000681.1:g.39071026G>A	GRCh37
NC_000019.8:g.43762866G>A	NCBI36
NG_008866.1:g.151687G>A , LRG_766:g.151687G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1464G>A
ENST00000688602.1:c.2861G>A
ENST00000689936.1:c.2833G>A
ENST00000359596.8:c.14528G>A MANE Select	ENSP00000352608.2:p.Gly4843Asp
ENST00000355481.8:c.14513G>A	ENSP00000347667.3:p.Gly4838Asp
ENST00000359596.7:c.14528G>A	ENSP00000352608.2:p.Gly4843Asp
ENST00000360985.7:c.14510G>A	ENSP00000354254.4:p.Gly4837Asp
NM_000540.2:c.14528G>A , LRG_766t1:c.14528G>A	NP_000531.2:p.Gly4843Asp
NM_001042723.1:c.14513G>A	NP_001036188.1:p.Gly4838Asp
XM_006723317.1:c.14510G>A	XP_006723380.1:p.Gly4837Asp
XM_006723319.1:c.14495G>A	XP_006723382.1:p.Gly4832Asp
XM_011527204.1:c.14525G>A	XP_011525506.1:p.Gly4842Asp
XM_011527205.1:c.14441G>A	XP_011525507.1:p.Gly4814Asp
XM_006723317.2:c.14510G>A	XP_006723380.1:p.Gly4837Asp
XM_006723319.2:c.14495G>A	XP_006723382.1:p.Gly4832Asp
XM_011527205.2:c.14441G>A	XP_011525507.1:p.Gly4814Asp
NM_000540.3:c.14528G>A MANE Select	NP_000531.2:p.Gly4843Asp
NM_001042723.2:c.14513G>A	NP_001036188.1:p.Gly4838Asp