Canonical Allele Identifier: CA405692734

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39076753T>C (hg19) ; chr19:g.38586113T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38586113T>C , CM000681.2:g.38586113T>C	GRCh38
NC_000019.9:g.39076753T>C , CM000681.1:g.39076753T>C	GRCh37
NC_000019.8:g.43768593T>C	NCBI36
NG_008866.1:g.157414T>C , LRG_766:g.157414T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1827T>C
ENST00000688602.1:c.3224T>C
ENST00000689936.1:c.3196T>C
ENST00000692547.1:n.284T>C
ENST00000359596.8:c.14891T>C MANE Select	ENSP00000352608.2:p.Ile4964Thr
ENST00000355481.8:c.14876T>C	ENSP00000347667.3:p.Ile4959Thr
ENST00000359596.7:c.14891T>C	ENSP00000352608.2:p.Ile4964Thr
ENST00000360985.7:c.14873T>C	ENSP00000354254.4:p.Ile4958Thr
NM_000540.2:c.14891T>C , LRG_766t1:c.14891T>C	NP_000531.2:p.Ile4964Thr
NM_001042723.1:c.14876T>C	NP_001036188.1:p.Ile4959Thr
XM_006723317.1:c.14873T>C	XP_006723380.1:p.Ile4958Thr
XM_006723319.1:c.14858T>C	XP_006723382.1:p.Ile4953Thr
XM_011527204.1:c.14888T>C	XP_011525506.1:p.Ile4963Thr
XM_011527205.1:c.14804T>C	XP_011525507.1:p.Ile4935Thr
XM_006723317.2:c.14873T>C	XP_006723380.1:p.Ile4958Thr
XM_006723319.2:c.14858T>C	XP_006723382.1:p.Ile4953Thr
XM_011527205.2:c.14804T>C	XP_011525507.1:p.Ile4935Thr
NM_000540.3:c.14891T>C MANE Select	NP_000531.2:p.Ile4964Thr
NM_001042723.2:c.14876T>C	NP_001036188.1:p.Ile4959Thr