Canonical Allele Identifier: CA405692599

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39076731A>G (hg19) ; chr19:g.38586091A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38586091A>G , CM000681.2:g.38586091A>G	GRCh38
NC_000019.9:g.39076731A>G , CM000681.1:g.39076731A>G	GRCh37
NC_000019.8:g.43768571A>G	NCBI36
NG_008866.1:g.157392A>G , LRG_766:g.157392A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1805A>G
ENST00000688602.1:c.3202A>G
ENST00000689936.1:c.3174A>G
ENST00000692547.1:n.262A>G
ENST00000359596.8:c.14869A>G MANE Select	ENSP00000352608.2:p.Thr4957Ala
ENST00000355481.8:c.14854A>G	ENSP00000347667.3:p.Thr4952Ala
ENST00000359596.7:c.14869A>G	ENSP00000352608.2:p.Thr4957Ala
ENST00000360985.7:c.14851A>G	ENSP00000354254.4:p.Thr4951Ala
NM_000540.2:c.14869A>G , LRG_766t1:c.14869A>G	NP_000531.2:p.Thr4957Ala
NM_001042723.1:c.14854A>G	NP_001036188.1:p.Thr4952Ala
XM_006723317.1:c.14851A>G	XP_006723380.1:p.Thr4951Ala
XM_006723319.1:c.14836A>G	XP_006723382.1:p.Thr4946Ala
XM_011527204.1:c.14866A>G	XP_011525506.1:p.Thr4956Ala
XM_011527205.1:c.14782A>G	XP_011525507.1:p.Thr4928Ala
XM_006723317.2:c.14851A>G	XP_006723380.1:p.Thr4951Ala
XM_006723319.2:c.14836A>G	XP_006723382.1:p.Thr4946Ala
XM_011527205.2:c.14782A>G	XP_011525507.1:p.Thr4928Ala
NM_000540.3:c.14869A>G MANE Select	NP_000531.2:p.Thr4957Ala
NM_001042723.2:c.14854A>G	NP_001036188.1:p.Thr4952Ala