Canonical Allele Identifier: CA405682649

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39063946C>T (hg19) ; chr19:g.38573306C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573306C>T , CM000681.2:g.38573306C>T	GRCh38
NC_000019.9:g.39063946C>T , CM000681.1:g.39063946C>T	GRCh37
NC_000019.8:g.43755786C>T	NCBI36
NG_008866.1:g.144607C>T , LRG_766:g.144607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1064C>T
ENST00000688602.1:c.2461C>T
ENST00000689936.1:c.2433C>T
ENST00000359596.8:c.14128C>T MANE Select	ENSP00000352608.2:p.Pro4710Ser
ENST00000355481.8:c.14113C>T	ENSP00000347667.3:p.Pro4705Ser
ENST00000359596.7:c.14128C>T	ENSP00000352608.2:p.Pro4710Ser
ENST00000360985.7:c.14110C>T	ENSP00000354254.4:p.Pro4704Ser
NM_000540.2:c.14128C>T , LRG_766t1:c.14128C>T	NP_000531.2:p.Pro4710Ser
NM_001042723.1:c.14113C>T	NP_001036188.1:p.Pro4705Ser
XM_006723317.1:c.14110C>T	XP_006723380.1:p.Pro4704Ser
XM_006723319.1:c.14095C>T	XP_006723382.1:p.Pro4699Ser
XM_011527204.1:c.14125C>T	XP_011525506.1:p.Pro4709Ser
XM_011527205.1:c.14041C>T	XP_011525507.1:p.Pro4681Ser
XM_006723317.2:c.14110C>T	XP_006723380.1:p.Pro4704Ser
XM_006723319.2:c.14095C>T	XP_006723382.1:p.Pro4699Ser
XM_011527205.2:c.14041C>T	XP_011525507.1:p.Pro4681Ser
NM_000540.3:c.14128C>T MANE Select	NP_000531.2:p.Pro4710Ser
NM_001042723.2:c.14113C>T	NP_001036188.1:p.Pro4705Ser