Canonical Allele Identifier: CA218895490

Gene: NELL1

Linked Data

• dbSNP Id: rs550058392
• MyVariant Identifiers: chr11:g.20805298A>T (hg19) ; chr11:g.20783752A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783752A>T , CM000673.2:g.20783752A>T	GRCh38
NC_000011.9:g.20805298A>T , CM000673.1:g.20805298A>T	GRCh37
NC_000011.8:g.20761874A>T	NCBI36
NG_047064.1:g.119202A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000357134.10:c.257A>T MANE Select	ENSP00000349654.5:p.Glu86Val
ENST00000298925.9:c.341A>T	ENSP00000298925.5:p.Glu114Val
ENST00000325319.9:c.257A>T	ENSP00000317837.5:p.Glu86Val
ENST00000357134.9:c.257A>T	ENSP00000349654.5:p.Glu86Val
ENST00000524738.1:n.84A>T
ENST00000527873.5:n.278A>T
ENST00000528046.5:n.440A>T
ENST00000529595.1:n.145A>T
ENST00000532434.5:c.257A>T	ENSP00000437170.1:p.Glu86Val
ENST00000619031.4:c.-456A>T	ENSP00000479479.1:n.-456A>T
NM_001288713.1:c.341A>T	NP_001275642.1:p.Glu114Val
NM_001288714.1:c.257A>T	NP_001275643.1:p.Glu86Val
NM_006157.4:c.257A>T	NP_006148.2:p.Glu86Val
NM_201551.2:c.257A>T	NP_963845.1:p.Glu86Val
NM_006157.5:c.257A>T MANE Select	NP_006148.2:p.Glu86Val