Canonical Allele Identifier: CA2769989708

Gene: SYCP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897278_10897280del , CM000668.2:g.10897278_10897280del	GRCh38
NC_000006.11:g.10897511_10897513del , CM000668.1:g.10897511_10897513del	GRCh37
NC_000006.10:g.11005497_11005499del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283141.11:c.337-733_337-731del MANE Select	ENSP00000283141.6:n.337-733_337-731del
ENST00000283141.10:c.337-733_337-731del	ENSP00000283141.6:n.337-733_337-731del
ENST00000341041.8:c.337-733_337-731del	ENSP00000340320.4:n.337-733_337-731del
ENST00000480294.1:c.*299-733_*299-731del	ENSP00000417929.1:n.*299-733_*299-731del
ENST00000543878.5:c.334-733_334-731del	ENSP00000440676.2:n.334-733_334-731del
NM_001040274.2:c.337-733_337-731del	NP_001035364.2:n.337-733_337-731del
NM_001040274.3:c.337-733_337-731del MANE Select	NP_001035364.2:n.337-733_337-731del