Canonical Allele Identifier: CA1610179557
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897085_10897086delinsGA , CM000668.2:g.10897085_10897086delinsGA GRCh38
NC_000006.11:g.10897318_10897319delinsGA , CM000668.1:g.10897318_10897319delinsGA GRCh37
NC_000006.10:g.11005304_11005305delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-926_337-925delinsGA MANE Select ENSP00000283141.6:n.337-926_337-925delins...
ENST00000283141.10:c.337-926_337-925delinsGA ENSP00000283141.6:n.337-926_337-925delins...
ENST00000341041.8:c.337-926_337-925delinsGA ENSP00000340320.4:n.337-926_337-925delins...
ENST00000480294.1:c.*299-926_*299-925delinsGA ENSP00000417929.1:n.*299-926_*299-925deli...
ENST00000543878.5:c.334-926_334-925delinsGA ENSP00000440676.2:n.334-926_334-925delins...
NM_001040274.2:c.337-926_337-925delinsGA NP_001035364.2:n.337-926_337-925delinsGA
NM_001040274.3:c.337-926_337-925delinsGA MANE Select NP_001035364.2:n.337-926_337-925delinsGA