Canonical Allele Identifier: CA1610179510

Gene: SYCP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897052_10897053delinsTC , CM000668.2:g.10897052_10897053delinsTC	GRCh38
NC_000006.11:g.10897285_10897286delinsTC , CM000668.1:g.10897285_10897286delinsTC	GRCh37
NC_000006.10:g.11005271_11005272delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000283141.11:c.337-959_337-958delinsTC MANE Select	ENSP00000283141.6:n.337-959_337-958delinsTC
ENST00000283141.10:c.337-959_337-958delinsTC	ENSP00000283141.6:n.337-959_337-958delinsTC
ENST00000341041.8:c.337-959_337-958delinsTC	ENSP00000340320.4:n.337-959_337-958delinsTC
ENST00000480294.1:c.*299-959_*299-958delinsTC	ENSP00000417929.1:n.*299-959_*299-958delinsTC
ENST00000543878.5:c.334-959_334-958delinsTC	ENSP00000440676.2:n.334-959_334-958delinsTC
NM_001040274.2:c.337-959_337-958delinsTC	NP_001035364.2:n.337-959_337-958delinsTC
NM_001040274.3:c.337-959_337-958delinsTC MANE Select	NP_001035364.2:n.337-959_337-958delinsTC