Canonical Allele Identifier: CA405681790

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063820C>G (hg19) ; chr19:g.38573180C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573180C>G , CM000681.2:g.38573180C>G	GRCh38
NC_000019.9:g.39063820C>G , CM000681.1:g.39063820C>G	GRCh37
NC_000019.8:g.43755660C>G	NCBI36
NG_008866.1:g.144481C>G , LRG_766:g.144481C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.938C>G
ENST00000688602.1:c.2335C>G
ENST00000689936.1:c.2307C>G
ENST00000359596.8:c.14002C>G MANE Select	ENSP00000352608.2:p.Pro4668Ala
ENST00000355481.8:c.13987C>G	ENSP00000347667.3:p.Pro4663Ala
ENST00000359596.7:c.14002C>G	ENSP00000352608.2:p.Pro4668Ala
ENST00000360985.7:c.13984C>G	ENSP00000354254.4:p.Pro4662Ala
NM_000540.2:c.14002C>G , LRG_766t1:c.14002C>G	NP_000531.2:p.Pro4668Ala
NM_001042723.1:c.13987C>G	NP_001036188.1:p.Pro4663Ala
XM_006723317.1:c.13984C>G	XP_006723380.1:p.Pro4662Ala
XM_006723319.1:c.13969C>G	XP_006723382.1:p.Pro4657Ala
XM_011527204.1:c.13999C>G	XP_011525506.1:p.Pro4667Ala
XM_011527205.1:c.13915C>G	XP_011525507.1:p.Pro4639Ala
XM_006723317.2:c.13984C>G	XP_006723380.1:p.Pro4662Ala
XM_006723319.2:c.13969C>G	XP_006723382.1:p.Pro4657Ala
XM_011527205.2:c.13915C>G	XP_011525507.1:p.Pro4639Ala
NM_000540.3:c.14002C>G MANE Select	NP_000531.2:p.Pro4668Ala
NM_001042723.2:c.13987C>G	NP_001036188.1:p.Pro4663Ala