Canonical Allele Identifier: CA405687690

Gene: RYR1

Linked Data

• MyVariant Identifiers: chr19:g.39071054C>G (hg19) ; chr19:g.38580414C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580414C>G , CM000681.2:g.38580414C>G	GRCh38
NC_000019.9:g.39071054C>G , CM000681.1:g.39071054C>G	GRCh37
NC_000019.8:g.43762894C>G	NCBI36
NG_008866.1:g.151715C>G , LRG_766:g.151715C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000593677.2:c.1492C>G
ENST00000688602.1:c.2889C>G
ENST00000689936.1:c.2861C>G
ENST00000359596.8:c.14556C>G MANE Select	ENSP00000352608.2:p.Tyr4852Ter
ENST00000355481.8:c.14541C>G	ENSP00000347667.3:p.Tyr4847Ter
ENST00000359596.7:c.14556C>G	ENSP00000352608.2:p.Tyr4852Ter
ENST00000360985.7:c.14538C>G	ENSP00000354254.4:p.Tyr4846Ter
NM_000540.2:c.14556C>G , LRG_766t1:c.14556C>G	NP_000531.2:p.Tyr4852Ter
NM_001042723.1:c.14541C>G	NP_001036188.1:p.Tyr4847Ter
XM_006723317.1:c.14538C>G	XP_006723380.1:p.Tyr4846Ter
XM_006723319.1:c.14523C>G	XP_006723382.1:p.Tyr4841Ter
XM_011527204.1:c.14553C>G	XP_011525506.1:p.Tyr4851Ter
XM_011527205.1:c.14469C>G	XP_011525507.1:p.Tyr4823Ter
XM_006723317.2:c.14538C>G	XP_006723380.1:p.Tyr4846Ter
XM_006723319.2:c.14523C>G	XP_006723382.1:p.Tyr4841Ter
XM_011527205.2:c.14469C>G	XP_011525507.1:p.Tyr4823Ter
NM_000540.3:c.14556C>G MANE Select	NP_000531.2:p.Tyr4852Ter
NM_001042723.2:c.14541C>G	NP_001036188.1:p.Tyr4847Ter