Canonical Allele Identifier: CA1956697985

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783681C= , CM000673.2:g.20783681C=	GRCh38
NC_000011.9:g.20805227C= , CM000673.1:g.20805227C=	GRCh37
NC_000011.8:g.20761803C=	NCBI36
NG_047064.1:g.119131C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.186C= MANE Select	ENSP00000349654.5:p.Asp62=
ENST00000298925.9:c.270C=	ENSP00000298925.5:p.Asp90=
ENST00000325319.9:c.186C=	ENSP00000317837.5:p.Asp62=
ENST00000357134.9:c.186C=	ENSP00000349654.5:p.Asp62=
ENST00000524738.1:n.13C=
ENST00000527873.5:n.207C=
ENST00000528046.5:n.369C=
ENST00000529595.1:n.74C=
ENST00000532434.5:c.186C=	ENSP00000437170.1:p.Asp62=
ENST00000619031.4:c.-527C=	ENSP00000479479.1:n.-527C=
NM_001288713.1:c.270C=	NP_001275642.1:p.Asp90=
NM_001288714.1:c.186C=	NP_001275643.1:p.Asp62=
NM_006157.4:c.186C=	NP_006148.2:p.Asp62=
NM_201551.2:c.186C=	NP_963845.1:p.Asp62=
NM_006157.5:c.186C= MANE Select	NP_006148.2:p.Asp62=