Canonical Allele Identifier: CA1610219418
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1780797977
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921343G>A , CM000668.2:g.10921343G>A GRCh38
NC_000006.11:g.10921576G>A , CM000668.1:g.10921576G>A GRCh37
NC_000006.10:g.11029562G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3153G>A MANE Select ENSP00000283141.6:n.1073-3153G>A
ENST00000283141.10:c.1073-3153G>A ENSP00000283141.6:n.1073-3153G>A
ENST00000341041.8:c.*151-1348G>A ENSP00000340320.4:n.*151-1348G>A
ENST00000480294.1:c.*1035-3153G>A ENSP00000417929.1:n.*1035-3153G>A
ENST00000487561.2:c.556-3153G>A ENSP00000417870.1:n.556-3153G>A
ENST00000543878.5:c.1070-3153G>A ENSP00000440676.2:n.1070-3153G>A
NM_001040274.2:c.1073-3153G>A NP_001035364.2:n.1073-3153G>A
NM_001040274.3:c.1073-3153G>A MANE Select NP_001035364.2:n.1073-3153G>A
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