Canonical Allele Identifier: CA1610219248
Gene: SYCP2L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921225G= , CM000668.2:g.10921225G= GRCh38
NC_000006.11:g.10921458G= , CM000668.1:g.10921458G= GRCh37
NC_000006.10:g.11029444G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3271G= MANE Select ENSP00000283141.6:n.1073-3271G=
ENST00000283141.10:c.1073-3271G= ENSP00000283141.6:n.1073-3271G=
ENST00000341041.8:c.*151-1466G= ENSP00000340320.4:n.*151-1466G=
ENST00000480294.1:c.*1035-3271G= ENSP00000417929.1:n.*1035-3271G=
ENST00000487561.2:c.556-3271G= ENSP00000417870.1:n.556-3271G=
ENST00000543878.5:c.1070-3271G= ENSP00000440676.2:n.1070-3271G=
NM_001040274.2:c.1073-3271G= NP_001035364.2:n.1073-3271G=
NM_001040274.3:c.1073-3271G= MANE Select NP_001035364.2:n.1073-3271G=
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