Canonical Allele Identifier: CA2528697114
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs2113339680

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921315_10921317del , CM000668.2:g.10921315_10921317del GRCh38
NC_000006.11:g.10921548_10921550del , CM000668.1:g.10921548_10921550del GRCh37
NC_000006.10:g.11029534_11029536del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3181_1073-3179del MANE Select ENSP00000283141.6:n.1073-3181_1073-3179de...
ENST00000283141.10:c.1073-3181_1073-3179del ENSP00000283141.6:n.1073-3181_1073-3179de...
ENST00000341041.8:c.*151-1376_*151-1374del ENSP00000340320.4:n.*151-1376_*151-1374de...
ENST00000480294.1:c.*1035-3181_*1035-3179del ENSP00000417929.1:n.*1035-3181_*1035-3179...
ENST00000487561.2:c.556-3181_556-3179del ENSP00000417870.1:n.556-3181_556-3179del
ENST00000543878.5:c.1070-3181_1070-3179del ENSP00000440676.2:n.1070-3181_1070-3179de...
NM_001040274.2:c.1073-3181_1073-3179del NP_001035364.2:n.1073-3181_1073-3179del
NM_001040274.3:c.1073-3181_1073-3179del MANE Select NP_001035364.2:n.1073-3181_1073-3179del