Canonical Allele Identifier: CA405687034

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39070677A>C (hg19) ; chr19:g.38580037A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580037A>C , CM000681.2:g.38580037A>C	GRCh38
NC_000019.9:g.39070677A>C , CM000681.1:g.39070677A>C	GRCh37
NC_000019.8:g.43762517A>C	NCBI36
NG_008866.1:g.151338A>C , LRG_766:g.151338A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1356A>C
ENST00000688602.1:c.2753A>C
ENST00000689936.1:c.2725A>C
ENST00000359596.8:c.14420A>C MANE Select	ENSP00000352608.2:p.Asn4807Thr
ENST00000355481.8:c.14405A>C	ENSP00000347667.3:p.Asn4802Thr
ENST00000359596.7:c.14420A>C	ENSP00000352608.2:p.Asn4807Thr
ENST00000360985.7:c.14402A>C	ENSP00000354254.4:p.Asn4801Thr
NM_000540.2:c.14420A>C , LRG_766t1:c.14420A>C	NP_000531.2:p.Asn4807Thr
NM_001042723.1:c.14405A>C	NP_001036188.1:p.Asn4802Thr
XM_006723317.1:c.14402A>C	XP_006723380.1:p.Asn4801Thr
XM_006723319.1:c.14387A>C	XP_006723382.1:p.Asn4796Thr
XM_011527204.1:c.14417A>C	XP_011525506.1:p.Asn4806Thr
XM_011527205.1:c.14333A>C	XP_011525507.1:p.Asn4778Thr
XM_006723317.2:c.14402A>C	XP_006723380.1:p.Asn4801Thr
XM_006723319.2:c.14387A>C	XP_006723382.1:p.Asn4796Thr
XM_011527205.2:c.14333A>C	XP_011525507.1:p.Asn4778Thr
NM_000540.3:c.14420A>C MANE Select	NP_000531.2:p.Asn4807Thr
NM_001042723.2:c.14405A>C	NP_001036188.1:p.Asn4802Thr