Canonical Allele Identifier: CA405662956

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39034490C>A (hg19) ; chr19:g.38543850C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543850C>A , CM000681.2:g.38543850C>A	GRCh38
NC_000019.9:g.39034490C>A , CM000681.1:g.39034490C>A	GRCh37
NC_000019.8:g.43726330C>A	NCBI36
NG_008866.1:g.115151C>A , LRG_766:g.115151C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.397C>A
ENST00000689936.1:c.379C>A
ENST00000359596.8:c.11987C>A MANE Select	ENSP00000352608.2:p.Ala3996Asp
ENST00000355481.8:c.11972C>A	ENSP00000347667.3:p.Ala3991Asp
ENST00000359596.7:c.11987C>A	ENSP00000352608.2:p.Ala3996Asp
ENST00000360985.7:c.11969C>A	ENSP00000354254.4:p.Ala3990Asp
ENST00000593322.1:c.596C>A
ENST00000594335.5:c.5356C>A
NM_000540.2:c.11987C>A , LRG_766t1:c.11987C>A	NP_000531.2:p.Ala3996Asp
NM_001042723.1:c.11972C>A	NP_001036188.1:p.Ala3991Asp
XM_006723317.1:c.11969C>A	XP_006723380.1:p.Ala3990Asp
XM_006723319.1:c.11954C>A	XP_006723382.1:p.Ala3985Asp
XM_011527204.1:c.11984C>A	XP_011525506.1:p.Ala3995Asp
XM_011527205.1:c.11987C>A	XP_011525507.1:p.Ala3996Asp
XM_006723317.2:c.11969C>A	XP_006723380.1:p.Ala3990Asp
XM_006723319.2:c.11954C>A	XP_006723382.1:p.Ala3985Asp
XM_011527205.2:c.11987C>A	XP_011525507.1:p.Ala3996Asp
NM_000540.3:c.11987C>A MANE Select	NP_000531.2:p.Ala3996Asp
NM_001042723.2:c.11972C>A	NP_001036188.1:p.Ala3991Asp