Canonical Allele Identifier: CA935817762

Gene: NELL1

Linked Data

• dbSNP Id: rs1856346764
• gnomAD v3: 11-21543509-CAGAATGGAG-C
• gnomAD v4: 11-21543509-CAGAATGGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.21543512_21543520del , CM000673.2:g.21543512_21543520del	GRCh38
NC_000011.9:g.21565058_21565066del , CM000673.1:g.21565058_21565066del	GRCh37
NC_000011.8:g.21521634_21521642del	NCBI36
NG_047064.1:g.878962_878970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.1786+8998_1786+9006del MANE Select	ENSP00000349654.5:n.1786+8998_1786+9006del
ENST00000298925.9:c.1870+8998_1870+9006del	ENSP00000298925.5:n.1870+8998_1870+9006del
ENST00000325319.9:c.1615+8998_1615+9006del	ENSP00000317837.5:n.1615+8998_1615+9006del
ENST00000357134.9:c.1786+8998_1786+9006del	ENSP00000349654.5:n.1786+8998_1786+9006del
ENST00000529218.5:n.1140+8998_1140+9006del
ENST00000532434.5:c.1646-16677_1646-16669del	ENSP00000437170.1:n.1646-16677_1646-16669del
ENST00000619031.4:c.1066+8998_1066+9006del	ENSP00000479479.1:n.1066+8998_1066+9006del
NM_001288713.1:c.1870+8998_1870+9006del	NP_001275642.1:n.1870+8998_1870+9006del
NM_001288714.1:c.1615+8998_1615+9006del	NP_001275643.1:n.1615+8998_1615+9006del
NM_006157.4:c.1786+8998_1786+9006del	NP_006148.2:n.1786+8998_1786+9006del
NM_201551.2:c.1646-16677_1646-16669del	NP_963845.1:n.1646-16677_1646-16669del
XM_011520119.1:c.829+8998_829+9006del	XP_011518421.1:n.829+8998_829+9006del
NM_006157.5:c.1786+8998_1786+9006del MANE Select	NP_006148.2:n.1786+8998_1786+9006del