Canonical Allele Identifier: CA380052663

Gene: NELL1

Linked Data

• gnomAD v4: 11-20783827-A-G
• MyVariant Identifiers: chr11:g.20805373A>G (hg19) ; chr11:g.20783827A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783827A>G , CM000673.2:g.20783827A>G	GRCh38
NC_000011.9:g.20805373A>G , CM000673.1:g.20805373A>G	GRCh37
NC_000011.8:g.20761949A>G	NCBI36
NG_047064.1:g.119277A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.332A>G MANE Select	ENSP00000349654.5:p.His111Arg
ENST00000298925.9:c.416A>G	ENSP00000298925.5:p.His139Arg
ENST00000325319.9:c.332A>G	ENSP00000317837.5:p.His111Arg
ENST00000357134.9:c.332A>G	ENSP00000349654.5:p.His111Arg
ENST00000524738.1:n.159A>G
ENST00000527873.5:n.353A>G
ENST00000528046.5:n.515A>G
ENST00000529595.1:n.220A>G
ENST00000532434.5:c.332A>G	ENSP00000437170.1:p.His111Arg
ENST00000619031.4:c.-381A>G	ENSP00000479479.1:n.-381A>G
NM_001288713.1:c.416A>G	NP_001275642.1:p.His139Arg
NM_001288714.1:c.332A>G	NP_001275643.1:p.His111Arg
NM_006157.4:c.332A>G	NP_006148.2:p.His111Arg
NM_201551.2:c.332A>G	NP_963845.1:p.His111Arg
NM_006157.5:c.332A>G MANE Select	NP_006148.2:p.His111Arg