Canonical Allele Identifier: CA1610179864

Gene: SYCP2L

Linked Data

• dbSNP Id: rs1780273173

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897288_10897290del , CM000668.2:g.10897288_10897290del	GRCh38
NC_000006.11:g.10897521_10897523del , CM000668.1:g.10897521_10897523del	GRCh37
NC_000006.10:g.11005507_11005509del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000283141.11:c.337-723_337-721del MANE Select	ENSP00000283141.6:n.337-723_337-721del
ENST00000283141.10:c.337-723_337-721del	ENSP00000283141.6:n.337-723_337-721del
ENST00000341041.8:c.337-723_337-721del	ENSP00000340320.4:n.337-723_337-721del
ENST00000480294.1:c.*299-723_*299-721del	ENSP00000417929.1:n.*299-723_*299-721del
ENST00000543878.5:c.334-723_334-721del	ENSP00000440676.2:n.334-723_334-721del
NM_001040274.2:c.337-723_337-721del	NP_001035364.2:n.337-723_337-721del
NM_001040274.3:c.337-723_337-721del MANE Select	NP_001035364.2:n.337-723_337-721del