Canonical Allele Identifier: CA1610179478

Gene: SYCP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897041_10897043delinsATT , CM000668.2:g.10897041_10897043delinsATT	GRCh38
NC_000006.11:g.10897274_10897276delinsATT , CM000668.1:g.10897274_10897276delinsATT	GRCh37
NC_000006.10:g.11005260_11005262delinsATT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000283141.11:c.337-970_337-968delinsATT MANE Select	ENSP00000283141.6:n.337-970_337-968delinsATT
ENST00000283141.10:c.337-970_337-968delinsATT	ENSP00000283141.6:n.337-970_337-968delinsATT
ENST00000341041.8:c.337-970_337-968delinsATT	ENSP00000340320.4:n.337-970_337-968delinsATT
ENST00000480294.1:c.*299-970_*299-968delinsATT	ENSP00000417929.1:n.*299-970_*299-968delinsATT
ENST00000543878.5:c.334-970_334-968delinsATT	ENSP00000440676.2:n.334-970_334-968delinsATT
NM_001040274.2:c.337-970_337-968delinsATT	NP_001035364.2:n.337-970_337-968delinsATT
NM_001040274.3:c.337-970_337-968delinsATT MANE Select	NP_001035364.2:n.337-970_337-968delinsATT