Canonical Allele Identifier: CA2561325104
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897016T>C , CM000668.2:g.10897016T>C GRCh38
NC_000006.11:g.10897249T>C , CM000668.1:g.10897249T>C GRCh37
NC_000006.10:g.11005235T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000283141.11:c.337-995T>C MANE Select ENSP00000283141.6:n.337-995T>C
ENST00000283141.10:c.337-995T>C ENSP00000283141.6:n.337-995T>C
ENST00000341041.8:c.337-995T>C ENSP00000340320.4:n.337-995T>C
ENST00000480294.1:c.*299-995T>C ENSP00000417929.1:n.*299-995T>C
ENST00000543878.5:c.334-995T>C ENSP00000440676.2:n.334-995T>C
NM_001040274.2:c.337-995T>C NP_001035364.2:n.337-995T>C
NM_001040274.3:c.337-995T>C MANE Select NP_001035364.2:n.337-995T>C