Canonical Allele Identifier: CA405687585

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071020C>A (hg19) ; chr19:g.38580380C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580380C>A , CM000681.2:g.38580380C>A	GRCh38
NC_000019.9:g.39071020C>A , CM000681.1:g.39071020C>A	GRCh37
NC_000019.8:g.43762860C>A	NCBI36
NG_008866.1:g.151681C>A , LRG_766:g.151681C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1458C>A
ENST00000688602.1:c.2855C>A
ENST00000689936.1:c.2827C>A
ENST00000359596.8:c.14522C>A MANE Select	ENSP00000352608.2:p.Thr4841Asn
ENST00000355481.8:c.14507C>A	ENSP00000347667.3:p.Thr4836Asn
ENST00000359596.7:c.14522C>A	ENSP00000352608.2:p.Thr4841Asn
ENST00000360985.7:c.14504C>A	ENSP00000354254.4:p.Thr4835Asn
NM_000540.2:c.14522C>A , LRG_766t1:c.14522C>A	NP_000531.2:p.Thr4841Asn
NM_001042723.1:c.14507C>A	NP_001036188.1:p.Thr4836Asn
XM_006723317.1:c.14504C>A	XP_006723380.1:p.Thr4835Asn
XM_006723319.1:c.14489C>A	XP_006723382.1:p.Thr4830Asn
XM_011527204.1:c.14519C>A	XP_011525506.1:p.Thr4840Asn
XM_011527205.1:c.14435C>A	XP_011525507.1:p.Thr4812Asn
XM_006723317.2:c.14504C>A	XP_006723380.1:p.Thr4835Asn
XM_006723319.2:c.14489C>A	XP_006723382.1:p.Thr4830Asn
XM_011527205.2:c.14435C>A	XP_011525507.1:p.Thr4812Asn
NM_000540.3:c.14522C>A MANE Select	NP_000531.2:p.Thr4841Asn
NM_001042723.2:c.14507C>A	NP_001036188.1:p.Thr4836Asn