Canonical Allele Identifier: CA15702820

Gene: NELL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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