Canonical Allele Identifier: CA1956697943

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783623_20783626delinsCCTT , CM000673.2:g.20783623_20783626delinsCCTT	GRCh38
NC_000011.9:g.20805169_20805172delinsCCTT , CM000673.1:g.20805169_20805172delinsCCTT	GRCh37
NC_000011.8:g.20761745_20761748delinsCCTT	NCBI36
NG_047064.1:g.119073_119076delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.185-57_185-54delinsCCTT MANE Select	ENSP00000349654.5:n.185-57_185-54delinsCCTT
ENST00000298925.9:c.269-57_269-54delinsCCTT	ENSP00000298925.5:n.269-57_269-54delinsCCTT
ENST00000325319.9:c.185-57_185-54delinsCCTT	ENSP00000317837.5:n.185-57_185-54delinsCCTT
ENST00000357134.9:c.185-57_185-54delinsCCTT	ENSP00000349654.5:n.185-57_185-54delinsCCTT
ENST00000527873.5:n.206-57_206-54delinsCCTT
ENST00000528046.5:n.368-57_368-54delinsCCTT
ENST00000529595.1:n.73-57_73-54delinsCCTT
ENST00000532434.5:c.185-57_185-54delinsCCTT	ENSP00000437170.1:n.185-57_185-54delinsCCTT
ENST00000619031.4:c.-528-57_-528-54delinsCCTT	ENSP00000479479.1:n.-528-57_-528-54delinsCCTT
NM_001288713.1:c.269-57_269-54delinsCCTT	NP_001275642.1:n.269-57_269-54delinsCCTT
NM_001288714.1:c.185-57_185-54delinsCCTT	NP_001275643.1:n.185-57_185-54delinsCCTT
NM_006157.4:c.185-57_185-54delinsCCTT	NP_006148.2:n.185-57_185-54delinsCCTT
NM_201551.2:c.185-57_185-54delinsCCTT	NP_963845.1:n.185-57_185-54delinsCCTT
NM_006157.5:c.185-57_185-54delinsCCTT MANE Select	NP_006148.2:n.185-57_185-54delinsCCTT