Canonical Allele Identifier: CA2584910344

Gene: RYR1

Linked Data

• gnomAD v4: 19-38573396-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573396T>G , CM000681.2:g.38573396T>G	GRCh38
NC_000019.9:g.39064036T>G , CM000681.1:g.39064036T>G	GRCh37
NC_000019.8:g.43755876T>G	NCBI36
NG_008866.1:g.144697T>G , LRG_766:g.144697T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1065+89T>G
ENST00000688602.1:c.2462+89T>G
ENST00000689936.1:c.2434+89T>G
ENST00000359596.8:c.14129+89T>G MANE Select	ENSP00000352608.2:n.14129+89T>G
ENST00000355481.8:c.14114+89T>G	ENSP00000347667.3:n.14114+89T>G
ENST00000359596.7:c.14129+89T>G	ENSP00000352608.2:n.14129+89T>G
ENST00000360985.7:c.14111+89T>G	ENSP00000354254.4:n.14111+89T>G
NM_000540.2:c.14129+89T>G , LRG_766t1:c.14129+89T>G	NP_000531.2:n.14129+89T>G
NM_001042723.1:c.14114+89T>G	NP_001036188.1:n.14114+89T>G
XM_006723317.1:c.14111+89T>G	XP_006723380.1:n.14111+89T>G
XM_006723319.1:c.14096+89T>G	XP_006723382.1:n.14096+89T>G
XM_011527204.1:c.14126+89T>G	XP_011525506.1:n.14126+89T>G
XM_011527205.1:c.14042+89T>G	XP_011525507.1:n.14042+89T>G
XM_006723317.2:c.14111+89T>G	XP_006723380.1:n.14111+89T>G
XM_006723319.2:c.14096+89T>G	XP_006723382.1:n.14096+89T>G
XM_011527205.2:c.14042+89T>G	XP_011525507.1:n.14042+89T>G
NM_000540.3:c.14129+89T>G MANE Select	NP_000531.2:n.14129+89T>G
NM_001042723.2:c.14114+89T>G	NP_001036188.1:n.14114+89T>G