Canonical Allele Identifier: CA1610180033

Gene: SYCP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897401_10897405delinsCACTT , CM000668.2:g.10897401_10897405delinsCACTT	GRCh38
NC_000006.11:g.10897634_10897638delinsCACTT , CM000668.1:g.10897634_10897638delinsCACTT	GRCh37
NC_000006.10:g.11005620_11005624delinsCACTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283141.11:c.337-610_337-606delinsCACTT MANE Select	ENSP00000283141.6:n.337-610_337-606delinsCACTT
ENST00000283141.10:c.337-610_337-606delinsCACTT	ENSP00000283141.6:n.337-610_337-606delinsCACTT
ENST00000341041.8:c.337-610_337-606delinsCACTT	ENSP00000340320.4:n.337-610_337-606delinsCACTT
ENST00000480294.1:c.*299-610_*299-606delinsCACTT	ENSP00000417929.1:n.*299-610_*299-606delinsCACTT
ENST00000543878.5:c.334-610_334-606delinsCACTT	ENSP00000440676.2:n.334-610_334-606delinsCACTT
NM_001040274.2:c.337-610_337-606delinsCACTT	NP_001035364.2:n.337-610_337-606delinsCACTT
NM_001040274.3:c.337-610_337-606delinsCACTT MANE Select	NP_001035364.2:n.337-610_337-606delinsCACTT