Canonical Allele Identifier: CA1956697833

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783390_20783391delinsCT , CM000673.2:g.20783390_20783391delinsCT	GRCh38
NC_000011.9:g.20804936_20804937delinsCT , CM000673.1:g.20804936_20804937delinsCT	GRCh37
NC_000011.8:g.20761512_20761513delinsCT	NCBI36
NG_047064.1:g.118840_118841delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.185-290_185-289delinsCT MANE Select	ENSP00000349654.5:n.185-290_185-289delinsCT
ENST00000298925.9:c.269-290_269-289delinsCT	ENSP00000298925.5:n.269-290_269-289delinsCT
ENST00000325319.9:c.185-290_185-289delinsCT	ENSP00000317837.5:n.185-290_185-289delinsCT
ENST00000357134.9:c.185-290_185-289delinsCT	ENSP00000349654.5:n.185-290_185-289delinsCT
ENST00000527873.5:n.206-290_206-289delinsCT
ENST00000528046.5:n.368-290_368-289delinsCT
ENST00000529595.1:n.73-290_73-289delinsCT
ENST00000532434.5:c.185-290_185-289delinsCT	ENSP00000437170.1:n.185-290_185-289delinsCT
ENST00000619031.4:c.-528-290_-528-289delinsCT	ENSP00000479479.1:n.-528-290_-528-289delinsCT
NM_001288713.1:c.269-290_269-289delinsCT	NP_001275642.1:n.269-290_269-289delinsCT
NM_001288714.1:c.185-290_185-289delinsCT	NP_001275643.1:n.185-290_185-289delinsCT
NM_006157.4:c.185-290_185-289delinsCT	NP_006148.2:n.185-290_185-289delinsCT
NM_201551.2:c.185-290_185-289delinsCT	NP_963845.1:n.185-290_185-289delinsCT
NM_006157.5:c.185-290_185-289delinsCT MANE Select	NP_006148.2:n.185-290_185-289delinsCT