Canonical Allele Identifier: CA2769989705

Gene: SYCP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897056A>T , CM000668.2:g.10897056A>T	GRCh38
NC_000006.11:g.10897289A>T , CM000668.1:g.10897289A>T	GRCh37
NC_000006.10:g.11005275A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283141.11:c.337-955A>T MANE Select	ENSP00000283141.6:n.337-955A>T
ENST00000283141.10:c.337-955A>T	ENSP00000283141.6:n.337-955A>T
ENST00000341041.8:c.337-955A>T	ENSP00000340320.4:n.337-955A>T
ENST00000480294.1:c.*299-955A>T	ENSP00000417929.1:n.*299-955A>T
ENST00000543878.5:c.334-955A>T	ENSP00000440676.2:n.334-955A>T
NM_001040274.2:c.337-955A>T	NP_001035364.2:n.337-955A>T
NM_001040274.3:c.337-955A>T MANE Select	NP_001035364.2:n.337-955A>T