Canonical Allele Identifier: CA935817771

Gene: NELL1

Linked Data

• dbSNP Id: rs1856347145
• gnomAD v3: 11-21543518-G-GAGGT
• gnomAD v4: 11-21543518-G-GAGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.21543519_21543522dup , CM000673.2:g.21543519_21543522dup	GRCh38
NC_000011.9:g.21565065_21565068dup , CM000673.1:g.21565065_21565068dup	GRCh37
NC_000011.8:g.21521641_21521644dup	NCBI36
NG_047064.1:g.878969_878972dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.1786+9005_1786+9008dup MANE Select	ENSP00000349654.5:n.1786+9005_1786+9008dup
ENST00000298925.9:c.1870+9005_1870+9008dup	ENSP00000298925.5:n.1870+9005_1870+9008dup
ENST00000325319.9:c.1615+9005_1615+9008dup	ENSP00000317837.5:n.1615+9005_1615+9008dup
ENST00000357134.9:c.1786+9005_1786+9008dup	ENSP00000349654.5:n.1786+9005_1786+9008dup
ENST00000529218.5:n.1140+9005_1140+9008dup
ENST00000532434.5:c.1646-16670_1646-16667dup	ENSP00000437170.1:n.1646-16670_1646-16667dup
ENST00000619031.4:c.1066+9005_1066+9008dup	ENSP00000479479.1:n.1066+9005_1066+9008dup
NM_001288713.1:c.1870+9005_1870+9008dup	NP_001275642.1:n.1870+9005_1870+9008dup
NM_001288714.1:c.1615+9005_1615+9008dup	NP_001275643.1:n.1615+9005_1615+9008dup
NM_006157.4:c.1786+9005_1786+9008dup	NP_006148.2:n.1786+9005_1786+9008dup
NM_201551.2:c.1646-16670_1646-16667dup	NP_963845.1:n.1646-16670_1646-16667dup
XM_011520119.1:c.829+9005_829+9008dup	XP_011518421.1:n.829+9005_829+9008dup
NM_006157.5:c.1786+9005_1786+9008dup MANE Select	NP_006148.2:n.1786+9005_1786+9008dup