Canonical Allele Identifier: CA405669476

Gene: RYR1

Linked Data

• COSMIC: COSM4131785
• MyVariant Identifiers: chr19:g.39051991G>A (hg19) ; chr19:g.38561351G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38561351G>A , CM000681.2:g.38561351G>A	GRCh38
NC_000019.9:g.39051991G>A , CM000681.1:g.39051991G>A	GRCh37
NC_000019.8:g.43743831G>A	NCBI36
NG_008866.1:g.132652G>A , LRG_766:g.132652G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000688602.1:c.931G>A
ENST00000689936.1:c.913G>A
ENST00000359596.8:c.12521G>A MANE Select	ENSP00000352608.2:p.Arg4174His
ENST00000355481.8:c.12506G>A	ENSP00000347667.3:p.Arg4169His
ENST00000359596.7:c.12521G>A	ENSP00000352608.2:p.Arg4174His
ENST00000360985.7:c.12503G>A	ENSP00000354254.4:p.Arg4168His
ENST00000594335.5:c.5890G>A
NM_000540.2:c.12521G>A , LRG_766t1:c.12521G>A	NP_000531.2:p.Arg4174His
NM_001042723.1:c.12506G>A	NP_001036188.1:p.Arg4169His
XM_006723317.1:c.12503G>A	XP_006723380.1:p.Arg4168His
XM_006723319.1:c.12488G>A	XP_006723382.1:p.Arg4163His
XM_011527204.1:c.12518G>A	XP_011525506.1:p.Arg4173His
XM_011527205.1:c.12521G>A	XP_011525507.1:p.Arg4174His
XM_006723317.2:c.12503G>A	XP_006723380.1:p.Arg4168His
XM_006723319.2:c.12488G>A	XP_006723382.1:p.Arg4163His
XM_011527205.2:c.12521G>A	XP_011525507.1:p.Arg4174His
NM_000540.3:c.12521G>A MANE Select	NP_000531.2:p.Arg4174His
NM_001042723.2:c.12506G>A	NP_001036188.1:p.Arg4169His