Canonical Allele Identifier: CA1956630659

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20677383C= , CM000673.2:g.20677383C=	GRCh38
NC_000011.9:g.20698929C= , CM000673.1:g.20698929C=	GRCh37
NC_000011.8:g.20655505C=	NCBI36
NG_047064.1:g.12833C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006157.5:c.56-549C= MANE Select	NP_006148.2:n.56-549C=
ENST00000357134.10:c.56-549C= MANE Select	ENSP00000349654.5:n.56-549C=
NM_001288713.1:c.140-549C=	NP_001275642.1:n.140-549C=
NM_001288714.1:c.56-549C=	NP_001275643.1:n.56-549C=
NM_006157.4:c.56-549C=	NP_006148.2:n.56-549C=
NM_201551.2:c.56-549C=	NP_963845.1:n.56-549C=
ENST00000298925.9:c.140-549C=	ENSP00000298925.5:n.140-549C=
ENST00000325319.9:c.56-549C=	ENSP00000317837.5:n.56-549C=
ENST00000357134.9:c.56-549C=	ENSP00000349654.5:n.56-549C=
ENST00000532434.5:c.56-549C=	ENSP00000437170.1:n.56-549C=