Canonical Allele Identifier: CA2507779315

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.21543526_21543527insTGGCATCTGCCTT , CM000673.2:g.21543526_21543527insTGGCATCTGCCTT	GRCh38
NC_000011.9:g.21565072_21565073insTGGCATCTGCCTT , CM000673.1:g.21565072_21565073insTGGCATCTGCCTT	GRCh37
NC_000011.8:g.21521648_21521649insTGGCATCTGCCTT	NCBI36
NG_047064.1:g.878976_878977insTGGCATCTGCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.1786+9012_1786+9013insTGGCATCTGCCTT MANE Select	ENSP00000349654.5:n.1786+9012_1786+9013insTGGCATCTGCCTT
ENST00000298925.9:c.1870+9012_1870+9013insTGGCATCTGCCTT	ENSP00000298925.5:n.1870+9012_1870+9013insTGGCATCTGCCTT
ENST00000325319.9:c.1615+9012_1615+9013insTGGCATCTGCCTT	ENSP00000317837.5:n.1615+9012_1615+9013insTGGCATCTGCCTT
ENST00000357134.9:c.1786+9012_1786+9013insTGGCATCTGCCTT	ENSP00000349654.5:n.1786+9012_1786+9013insTGGCATCTGCCTT
ENST00000529218.5:n.1140+9012_1140+9013insTGGCATCTGCCTT
ENST00000532434.5:c.1646-16663_1646-16662insTGGCATCTGCCTT	ENSP00000437170.1:n.1646-16663_1646-16662insTGGCATCTGCCTT
ENST00000619031.4:c.1066+9012_1066+9013insTGGCATCTGCCTT	ENSP00000479479.1:n.1066+9012_1066+9013insTGGCATCTGCCTT
NM_001288713.1:c.1870+9012_1870+9013insTGGCATCTGCCTT	NP_001275642.1:n.1870+9012_1870+9013insTGGCATCTGCCTT
NM_001288714.1:c.1615+9012_1615+9013insTGGCATCTGCCTT	NP_001275643.1:n.1615+9012_1615+9013insTGGCATCTGCCTT
NM_006157.4:c.1786+9012_1786+9013insTGGCATCTGCCTT	NP_006148.2:n.1786+9012_1786+9013insTGGCATCTGCCTT
NM_201551.2:c.1646-16663_1646-16662insTGGCATCTGCCTT	NP_963845.1:n.1646-16663_1646-16662insTGGCATCTGCCTT
XM_011520119.1:c.829+9012_829+9013insTGGCATCTGCCTT	XP_011518421.1:n.829+9012_829+9013insTGGCATCTGCCTT
NM_006157.5:c.1786+9012_1786+9013insTGGCATCTGCCTT MANE Select	NP_006148.2:n.1786+9012_1786+9013insTGGCATCTGCCTT