Canonical Allele Identifier: CA674589467

Gene: NELL1

Linked Data

• dbSNP Id: rs1257855770
• gnomAD v3: 11-21543396-AT-A
• gnomAD v4: 11-21543396-AT-A
• MyVariant Identifiers: chr11:g.21564943del (hg19) ; chr11:g.21543397del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.21543397del , CM000673.2:g.21543397del	GRCh38
NC_000011.9:g.21564943del , CM000673.1:g.21564943del	GRCh37
NC_000011.8:g.21521519del	NCBI36
NG_047064.1:g.878847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.1786+8883del MANE Select	ENSP00000349654.5:n.1786+8883del
ENST00000298925.9:c.1870+8883del	ENSP00000298925.5:n.1870+8883del
ENST00000325319.9:c.1615+8883del	ENSP00000317837.5:n.1615+8883del
ENST00000357134.9:c.1786+8883del	ENSP00000349654.5:n.1786+8883del
ENST00000529218.5:n.1140+8883del
ENST00000532434.5:c.1646-16792del	ENSP00000437170.1:n.1646-16792del
ENST00000619031.4:c.1066+8883del	ENSP00000479479.1:n.1066+8883del
NM_001288713.1:c.1870+8883del	NP_001275642.1:n.1870+8883del
NM_001288714.1:c.1615+8883del	NP_001275643.1:n.1615+8883del
NM_006157.4:c.1786+8883del	NP_006148.2:n.1786+8883del
NM_201551.2:c.1646-16792del	NP_963845.1:n.1646-16792del
XM_011520119.1:c.829+8883del	XP_011518421.1:n.829+8883del
NM_006157.5:c.1786+8883del MANE Select	NP_006148.2:n.1786+8883del