Canonical Allele Identifier: CA1610179502
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897050T= , CM000668.2:g.10897050T= GRCh38
NC_000006.11:g.10897283T= , CM000668.1:g.10897283T= GRCh37
NC_000006.10:g.11005269T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000283141.11:c.337-961T= MANE Select ENSP00000283141.6:n.337-961T=
ENST00000283141.10:c.337-961T= ENSP00000283141.6:n.337-961T=
ENST00000341041.8:c.337-961T= ENSP00000340320.4:n.337-961T=
ENST00000480294.1:c.*299-961T= ENSP00000417929.1:n.*299-961T=
ENST00000543878.5:c.334-961T= ENSP00000440676.2:n.334-961T=
NM_001040274.2:c.337-961T= NP_001035364.2:n.337-961T=
NM_001040274.3:c.337-961T= MANE Select NP_001035364.2:n.337-961T=