Canonical Allele Identifier: CA1610179899
Gene: SYCP2L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897312A= , CM000668.2:g.10897312A= GRCh38
NC_000006.11:g.10897545A= , CM000668.1:g.10897545A= GRCh37
NC_000006.10:g.11005531A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-699A= MANE Select ENSP00000283141.6:n.337-699A=
ENST00000283141.10:c.337-699A= ENSP00000283141.6:n.337-699A=
ENST00000341041.8:c.337-699A= ENSP00000340320.4:n.337-699A=
ENST00000480294.1:c.*299-699A= ENSP00000417929.1:n.*299-699A=
ENST00000543878.5:c.334-699A= ENSP00000440676.2:n.334-699A=
NM_001040274.2:c.337-699A= NP_001035364.2:n.337-699A=
NM_001040274.3:c.337-699A= MANE Select NP_001035364.2:n.337-699A=
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