Canonical Allele Identifier: CA507356072

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39062778C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572138C>A , CM000681.2:g.38572138C>A	GRCh38
NC_000019.9:g.39062778C>A , CM000681.1:g.39062778C>A	GRCh37
NC_000019.8:g.43754618C>A	NCBI36
NG_008866.1:g.143439C>A , LRG_766:g.143439C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.802C>A
ENST00000688602.1:c.2199C>A
ENST00000689936.1:c.2171C>A
ENST00000359596.8:c.13866C>A MANE Select	ENSP00000352608.2:p.Gly4622=
ENST00000355481.8:c.13851C>A	ENSP00000347667.3:p.Gly4617=
ENST00000359596.7:c.13866C>A	ENSP00000352608.2:p.Gly4622=
ENST00000360985.7:c.13848C>A	ENSP00000354254.4:p.Gly4616=
ENST00000593677.1:c.326C>A
NM_000540.2:c.13866C>A , LRG_766t1:c.13866C>A	NP_000531.2:p.Gly4622=
NM_001042723.1:c.13851C>A	NP_001036188.1:p.Gly4617=
XM_006723317.1:c.13848C>A	XP_006723380.1:p.Gly4616=
XM_006723319.1:c.13833C>A	XP_006723382.1:p.Gly4611=
XM_011527204.1:c.13863C>A	XP_011525506.1:p.Gly4621=
XM_011527205.1:c.13779C>A	XP_011525507.1:p.Gly4593=
XM_006723317.2:c.13848C>A	XP_006723380.1:p.Gly4616=
XM_006723319.2:c.13833C>A	XP_006723382.1:p.Gly4611=
XM_011527205.2:c.13779C>A	XP_011525507.1:p.Gly4593=
NM_000540.3:c.13866C>A MANE Select	NP_000531.2:p.Gly4622=
NM_001042723.2:c.13851C>A	NP_001036188.1:p.Gly4617=