Canonical Allele Identifier: CA1610179682
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897209_10897210delinsTA , CM000668.2:g.10897209_10897210delinsTA GRCh38
NC_000006.11:g.10897442_10897443delinsTA , CM000668.1:g.10897442_10897443delinsTA GRCh37
NC_000006.10:g.11005428_11005429delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-802_337-801delinsTA MANE Select ENSP00000283141.6:n.337-802_337-801delins...
ENST00000283141.10:c.337-802_337-801delinsTA ENSP00000283141.6:n.337-802_337-801delins...
ENST00000341041.8:c.337-802_337-801delinsTA ENSP00000340320.4:n.337-802_337-801delins...
ENST00000480294.1:c.*299-802_*299-801delinsTA ENSP00000417929.1:n.*299-802_*299-801deli...
ENST00000543878.5:c.334-802_334-801delinsTA ENSP00000440676.2:n.334-802_334-801delins...
NM_001040274.2:c.337-802_337-801delinsTA NP_001035364.2:n.337-802_337-801delinsTA
NM_001040274.3:c.337-802_337-801delinsTA MANE Select NP_001035364.2:n.337-802_337-801delinsTA