Canonical Allele Identifier: CA405687872

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071092A>T (hg19) ; chr19:g.38580452A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580452A>T , CM000681.2:g.38580452A>T	GRCh38
NC_000019.9:g.39071092A>T , CM000681.1:g.39071092A>T	GRCh37
NC_000019.8:g.43762932A>T	NCBI36
NG_008866.1:g.151753A>T , LRG_766:g.151753A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1530A>T
ENST00000688602.1:c.2927A>T
ENST00000689936.1:c.2899A>T
ENST00000359596.8:c.14594A>T MANE Select	ENSP00000352608.2:p.Asn4865Ile
ENST00000355481.8:c.14579A>T	ENSP00000347667.3:p.Asn4860Ile
ENST00000359596.7:c.14594A>T	ENSP00000352608.2:p.Asn4865Ile
ENST00000360985.7:c.14576A>T	ENSP00000354254.4:p.Asn4859Ile
NM_000540.2:c.14594A>T , LRG_766t1:c.14594A>T	NP_000531.2:p.Asn4865Ile
NM_001042723.1:c.14579A>T	NP_001036188.1:p.Asn4860Ile
XM_006723317.1:c.14576A>T	XP_006723380.1:p.Asn4859Ile
XM_006723319.1:c.14561A>T	XP_006723382.1:p.Asn4854Ile
XM_011527204.1:c.14591A>T	XP_011525506.1:p.Asn4864Ile
XM_011527205.1:c.14507A>T	XP_011525507.1:p.Asn4836Ile
XM_006723317.2:c.14576A>T	XP_006723380.1:p.Asn4859Ile
XM_006723319.2:c.14561A>T	XP_006723382.1:p.Asn4854Ile
XM_011527205.2:c.14507A>T	XP_011525507.1:p.Asn4836Ile
NM_000540.3:c.14594A>T MANE Select	NP_000531.2:p.Asn4865Ile
NM_001042723.2:c.14579A>T	NP_001036188.1:p.Asn4860Ile