Canonical Allele Identifier: CA2790639579
Gene: CSRP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188199_19188200insGGCAACGTAGGCTGAGTTGGATTTCGGCGAAAGGGCTAGATCGATGACGATGTTGGCGATGAGAATGCGGGCCTCAGG , CM000673.2:g.19188199_19188200insGGCAACGTAGGCTGAGTTGGATTTCGGCGAAAGGGCTAGATCGATGACGATGTTGGCGATGAGAATGCGGGCCTCAGG GRCh38
NC_000011.9:g.19209746_19209747insGGCAACGTAGGCTGAGTTGGATTTCGGCGAAAGGGCTAGATCGATGACGATGTTGGCGATGAGAATGCGGGCCTCAGG , CM000673.1:g.19209746_19209747insGGCAACGTAGGCTGAGTTGGATTTCGGCGAAAGGGCTAGATCGATGACGATGTTGGCGATGAGAATGCGGGCCTCAGG GRCh37
NC_000011.8:g.19166322_19166323insGGCAACGTAGGCTGAGTTGGATTTCGGCGAAAGGGCTAGATCGATGACGATGTTGGCGATGAGAATGCGGGCCTCAGG NCBI36
NG_011932.2:g.27374_27375insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC , LRG_440:g.27374_27375insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC MANE Select ENSP00000265968.3:p.Tyr73SerfsTer2
ENST00000533783.2:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC ENSP00000431813.1:p.Tyr73SerfsTer2
ENST00000647990.1:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC ENSP00000496798.1:p.Tyr73SerfsTer2
ENST00000648719.1:c.113-3155_113-3154insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC ENSP00000497633.1:n.113-3155_113-3154insCCTGAGGCCCGCATTCTCATC...
ENST00000649235.1:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC ENSP00000497388.1:p.Tyr73SerfsTer2
ENST00000649842.1:c.113-1852_113-1851insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC ENSP00000497531.1:n.113-1852_113-1851insCCTGAGGCCCGCATTCTCATC...
ENST00000265968.7:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC ENSP00000265968.3:p.Tyr73SerfsTer2
ENST00000533783.1:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC ENSP00000431813.1:p.Tyr73SerfsTer2
NM_003476.4:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC NP_003467.1:p.Tyr73SerfsTer2
XM_024448698.1:c.113-1852_113-1851insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC XP_024304466.1:n.113-1852_113-1851insCCTGAGGCCCGCATTCTCATCGCC...
NM_001369404.1:c.113-1852_113-1851insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC NP_001356333.1:n.113-1852_113-1851insCCTGAGGCCCGCATTCTCATCGCC...
NM_003476.5:c.217_218insCCTGAGGCCCGCATTCTCATCGCCAACATCGTCATCGATCTAGCCCTTTCGCCGAAATCCAACTCAGCCTACGTTGCC MANE Select NP_003467.1:p.Tyr73SerfsTer2
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