Canonical Allele Identifier: CA405673735

Gene: RYR1

Linked Data

• gnomAD v4: 19-38565484-C-A
• MyVariant Identifiers: chr19:g.39056124C>A (hg19) ; chr19:g.38565484C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565484C>A , CM000681.2:g.38565484C>A	GRCh38
NC_000019.9:g.39056124C>A , CM000681.1:g.39056124C>A	GRCh37
NC_000019.8:g.43747964C>A	NCBI36
NG_008866.1:g.136785C>A , LRG_766:g.136785C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.86C>A
ENST00000688602.1:c.1560C>A
ENST00000689936.1:c.1542C>A
ENST00000359596.8:c.13150C>A MANE Select	ENSP00000352608.2:p.Pro4384Thr
ENST00000355481.8:c.13135C>A	ENSP00000347667.3:p.Pro4379Thr
ENST00000359596.7:c.13150C>A	ENSP00000352608.2:p.Pro4384Thr
ENST00000360985.7:c.13132C>A	ENSP00000354254.4:p.Pro4378Thr
NM_000540.2:c.13150C>A , LRG_766t1:c.13150C>A	NP_000531.2:p.Pro4384Thr
NM_001042723.1:c.13135C>A	NP_001036188.1:p.Pro4379Thr
XM_006723317.1:c.13132C>A	XP_006723380.1:p.Pro4378Thr
XM_006723319.1:c.13117C>A	XP_006723382.1:p.Pro4373Thr
XM_011527204.1:c.13147C>A	XP_011525506.1:p.Pro4383Thr
XM_011527205.1:c.13150C>A	XP_011525507.1:p.Pro4384Thr
XM_006723317.2:c.13132C>A	XP_006723380.1:p.Pro4378Thr
XM_006723319.2:c.13117C>A	XP_006723382.1:p.Pro4373Thr
XM_011527205.2:c.13150C>A	XP_011525507.1:p.Pro4384Thr
NM_000540.3:c.13150C>A MANE Select	NP_000531.2:p.Pro4384Thr
NM_001042723.2:c.13135C>A	NP_001036188.1:p.Pro4379Thr