Canonical Allele Identifier: CA1610179905
Gene: SYCP2L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897313_10897314delinsCT , CM000668.2:g.10897313_10897314delinsCT GRCh38
NC_000006.11:g.10897546_10897547delinsCT , CM000668.1:g.10897546_10897547delinsCT GRCh37
NC_000006.10:g.11005532_11005533delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-698_337-697delinsCT MANE Select ENSP00000283141.6:n.337-698_337-697delins...
ENST00000283141.10:c.337-698_337-697delinsCT ENSP00000283141.6:n.337-698_337-697delins...
ENST00000341041.8:c.337-698_337-697delinsCT ENSP00000340320.4:n.337-698_337-697delins...
ENST00000480294.1:c.*299-698_*299-697delinsCT ENSP00000417929.1:n.*299-698_*299-697deli...
ENST00000543878.5:c.334-698_334-697delinsCT ENSP00000440676.2:n.334-698_334-697delins...
NM_001040274.2:c.337-698_337-697delinsCT NP_001035364.2:n.337-698_337-697delinsCT
NM_001040274.3:c.337-698_337-697delinsCT MANE Select NP_001035364.2:n.337-698_337-697delinsCT
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