Canonical Allele Identifier: CA405673510

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565445G>T , CM000681.2:g.38565445G>T	GRCh38
NC_000019.9:g.39056085G>T , CM000681.1:g.39056085G>T	GRCh37
NC_000019.8:g.43747925G>T	NCBI36
NG_008866.1:g.136746G>T , LRG_766:g.136746G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.13111G>T MANE Select	NP_000531.2:p.Ala4371Ser
ENST00000359596.8:c.13111G>T MANE Select	ENSP00000352608.2:p.Ala4371Ser
NM_000540.2:c.13111G>T , LRG_766t1:c.13111G>T	NP_000531.2:p.Ala4371Ser
NM_001042723.1:c.13096G>T	NP_001036188.1:p.Ala4366Ser
NM_001042723.2:c.13096G>T	NP_001036188.1:p.Ala4366Ser
ENST00000355481.8:c.13096G>T	ENSP00000347667.3:p.Ala4366Ser
ENST00000359596.7:c.13111G>T	ENSP00000352608.2:p.Ala4371Ser
ENST00000360985.7:c.13093G>T	ENSP00000354254.4:p.Ala4365Ser
ENST00000593677.2:c.47G>T
ENST00000688602.1:c.1521G>T
ENST00000689936.1:c.1503G>T
XM_006723317.1:c.13093G>T	XP_006723380.1:p.Ala4365Ser
XM_006723317.2:c.13093G>T	XP_006723380.1:p.Ala4365Ser
XM_006723319.1:c.13078G>T	XP_006723382.1:p.Ala4360Ser
XM_006723319.2:c.13078G>T	XP_006723382.1:p.Ala4360Ser
XM_011527204.1:c.13108G>T	XP_011525506.1:p.Ala4370Ser
XM_011527205.1:c.13111G>T	XP_011525507.1:p.Ala4371Ser
XM_011527205.2:c.13111G>T	XP_011525507.1:p.Ala4371Ser