Canonical Allele Identifier: CA2560492049
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897305_10897307del , CM000668.2:g.10897305_10897307del GRCh38
NC_000006.11:g.10897538_10897540del , CM000668.1:g.10897538_10897540del GRCh37
NC_000006.10:g.11005524_11005526del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-706_337-704del MANE Select ENSP00000283141.6:n.337-706_337-704del
ENST00000283141.10:c.337-706_337-704del ENSP00000283141.6:n.337-706_337-704del
ENST00000341041.8:c.337-706_337-704del ENSP00000340320.4:n.337-706_337-704del
ENST00000480294.1:c.*299-706_*299-704del ENSP00000417929.1:n.*299-706_*299-704del
ENST00000543878.5:c.334-706_334-704del ENSP00000440676.2:n.334-706_334-704del
NM_001040274.2:c.337-706_337-704del NP_001035364.2:n.337-706_337-704del
NM_001040274.3:c.337-706_337-704del MANE Select NP_001035364.2:n.337-706_337-704del