Canonical Allele Identifier: CA405681254

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39062854A>G (hg19) ; chr19:g.38572214A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572214A>G , CM000681.2:g.38572214A>G	GRCh38
NC_000019.9:g.39062854A>G , CM000681.1:g.39062854A>G	GRCh37
NC_000019.8:g.43754694A>G	NCBI36
NG_008866.1:g.143515A>G , LRG_766:g.143515A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.878A>G
ENST00000688602.1:c.2275A>G
ENST00000689936.1:c.2247A>G
ENST00000359596.8:c.13942A>G MANE Select	ENSP00000352608.2:p.Ser4648Gly
ENST00000355481.8:c.13927A>G	ENSP00000347667.3:p.Ser4643Gly
ENST00000359596.7:c.13942A>G	ENSP00000352608.2:p.Ser4648Gly
ENST00000360985.7:c.13924A>G	ENSP00000354254.4:p.Ser4642Gly
ENST00000593677.1:c.402A>G
NM_000540.2:c.13942A>G , LRG_766t1:c.13942A>G	NP_000531.2:p.Ser4648Gly
NM_001042723.1:c.13927A>G	NP_001036188.1:p.Ser4643Gly
XM_006723317.1:c.13924A>G	XP_006723380.1:p.Ser4642Gly
XM_006723319.1:c.13909A>G	XP_006723382.1:p.Ser4637Gly
XM_011527204.1:c.13939A>G	XP_011525506.1:p.Ser4647Gly
XM_011527205.1:c.13855A>G	XP_011525507.1:p.Ser4619Gly
XM_006723317.2:c.13924A>G	XP_006723380.1:p.Ser4642Gly
XM_006723319.2:c.13909A>G	XP_006723382.1:p.Ser4637Gly
XM_011527205.2:c.13855A>G	XP_011525507.1:p.Ser4619Gly
NM_000540.3:c.13942A>G MANE Select	NP_000531.2:p.Ser4648Gly
NM_001042723.2:c.13927A>G	NP_001036188.1:p.Ser4643Gly