Canonical Allele Identifier: CA1956698038

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783826C= , CM000673.2:g.20783826C=	GRCh38
NC_000011.9:g.20805372C= , CM000673.1:g.20805372C=	GRCh37
NC_000011.8:g.20761948C=	NCBI36
NG_047064.1:g.119276C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.331C= MANE Select	ENSP00000349654.5:p.His111=
ENST00000298925.9:c.415C=	ENSP00000298925.5:p.His139=
ENST00000325319.9:c.331C=	ENSP00000317837.5:p.His111=
ENST00000357134.9:c.331C=	ENSP00000349654.5:p.His111=
ENST00000524738.1:n.158C=
ENST00000527873.5:n.352C=
ENST00000528046.5:n.514C=
ENST00000529595.1:n.219C=
ENST00000532434.5:c.331C=	ENSP00000437170.1:p.His111=
ENST00000619031.4:c.-382C=	ENSP00000479479.1:n.-382C=
NM_001288713.1:c.415C=	NP_001275642.1:p.His139=
NM_001288714.1:c.331C=	NP_001275643.1:p.His111=
NM_006157.4:c.331C=	NP_006148.2:p.His111=
NM_201551.2:c.331C=	NP_963845.1:p.His111=
NM_006157.5:c.331C= MANE Select	NP_006148.2:p.His111=