Canonical Allele Identifier: CA380052484

Gene: NELL1

Linked Data

• MyVariant Identifiers: chr11:g.20805288A>G (hg19) ; chr11:g.20783742A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783742A>G , CM000673.2:g.20783742A>G	GRCh38
NC_000011.9:g.20805288A>G , CM000673.1:g.20805288A>G	GRCh37
NC_000011.8:g.20761864A>G	NCBI36
NG_047064.1:g.119192A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357134.10:c.247A>G MANE Select	ENSP00000349654.5:p.Asn83Asp
ENST00000298925.9:c.331A>G	ENSP00000298925.5:p.Asn111Asp
ENST00000325319.9:c.247A>G	ENSP00000317837.5:p.Asn83Asp
ENST00000357134.9:c.247A>G	ENSP00000349654.5:p.Asn83Asp
ENST00000524738.1:n.74A>G
ENST00000527873.5:n.268A>G
ENST00000528046.5:n.430A>G
ENST00000529595.1:n.135A>G
ENST00000532434.5:c.247A>G	ENSP00000437170.1:p.Asn83Asp
ENST00000619031.4:c.-466A>G	ENSP00000479479.1:n.-466A>G
NM_001288713.1:c.331A>G	NP_001275642.1:p.Asn111Asp
NM_001288714.1:c.247A>G	NP_001275643.1:p.Asn83Asp
NM_006157.4:c.247A>G	NP_006148.2:p.Asn83Asp
NM_201551.2:c.247A>G	NP_963845.1:p.Asn83Asp
NM_006157.5:c.247A>G MANE Select	NP_006148.2:p.Asn83Asp