Canonical Allele Identifier: CA1610179859
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897285_10897288delinsTTAC , CM000668.2:g.10897285_10897288delinsTTAC GRCh38
NC_000006.11:g.10897518_10897521delinsTTAC , CM000668.1:g.10897518_10897521delinsTTAC GRCh37
NC_000006.10:g.11005504_11005507delinsTTAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-726_337-723delinsTTAC MANE Select ENSP00000283141.6:n.337-726_337-723delins...
ENST00000283141.10:c.337-726_337-723delinsTTAC ENSP00000283141.6:n.337-726_337-723delins...
ENST00000341041.8:c.337-726_337-723delinsTTAC ENSP00000340320.4:n.337-726_337-723delins...
ENST00000480294.1:c.*299-726_*299-723delinsTTAC ENSP00000417929.1:n.*299-726_*299-723deli...
ENST00000543878.5:c.334-726_334-723delinsTTAC ENSP00000440676.2:n.334-726_334-723delins...
NM_001040274.2:c.337-726_337-723delinsTTAC NP_001035364.2:n.337-726_337-723delinsTTA...
NM_001040274.3:c.337-726_337-723delinsTTAC MANE Select NP_001035364.2:n.337-726_337-723delinsTTA...