Canonical Allele Identifier: CA1610179788
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897258_10897259delinsAG , CM000668.2:g.10897258_10897259delinsAG GRCh38
NC_000006.11:g.10897491_10897492delinsAG , CM000668.1:g.10897491_10897492delinsAG GRCh37
NC_000006.10:g.11005477_11005478delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-753_337-752delinsAG MANE Select ENSP00000283141.6:n.337-753_337-752delins...
ENST00000283141.10:c.337-753_337-752delinsAG ENSP00000283141.6:n.337-753_337-752delins...
ENST00000341041.8:c.337-753_337-752delinsAG ENSP00000340320.4:n.337-753_337-752delins...
ENST00000480294.1:c.*299-753_*299-752delinsAG ENSP00000417929.1:n.*299-753_*299-752deli...
ENST00000543878.5:c.334-753_334-752delinsAG ENSP00000440676.2:n.334-753_334-752delins...
NM_001040274.2:c.337-753_337-752delinsAG NP_001035364.2:n.337-753_337-752delinsAG
NM_001040274.3:c.337-753_337-752delinsAG MANE Select NP_001035364.2:n.337-753_337-752delinsAG