Canonical Allele Identifier: CA1956698129

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20784016G= , CM000673.2:g.20784016G=	GRCh38
NC_000011.9:g.20805562G= , CM000673.1:g.20805562G=	GRCh37
NC_000011.8:g.20762138G=	NCBI36
NG_047064.1:g.119466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.335+186G= MANE Select	ENSP00000349654.5:n.335+186G=
ENST00000298925.9:c.419+186G=	ENSP00000298925.5:n.419+186G=
ENST00000325319.9:c.335+186G=	ENSP00000317837.5:n.335+186G=
ENST00000357134.9:c.335+186G=	ENSP00000349654.5:n.335+186G=
ENST00000524738.1:n.162+186G=
ENST00000527873.5:n.356+186G=
ENST00000528046.5:n.518+186G=
ENST00000529595.1:n.223+186G=
ENST00000532434.5:c.335+186G=	ENSP00000437170.1:n.335+186G=
ENST00000619031.4:c.-378+186G=	ENSP00000479479.1:n.-378+186G=
NM_001288713.1:c.419+186G=	NP_001275642.1:n.419+186G=
NM_001288714.1:c.335+186G=	NP_001275643.1:n.335+186G=
NM_006157.4:c.335+186G=	NP_006148.2:n.335+186G=
NM_201551.2:c.335+186G=	NP_963845.1:n.335+186G=
NM_006157.5:c.335+186G= MANE Select	NP_006148.2:n.335+186G=