Canonical Allele Identifier: CA218895447

Gene: NELL1

Linked Data

• dbSNP Id: rs199754808
• gnomAD v2: 11-20804919-G-GT
• gnomAD v3: 11-20783373-G-GT
• gnomAD v4: 11-20783373-G-GT
• MyVariant Identifiers: chr11:g.20804920_20804921insT (hg19) ; chr11:g.20804919_20804920insT (hg19) ; chr11:g.20783374_20783375insT (hg38) ; chr11:g.20783373_20783374insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783374dup , CM000673.2:g.20783374dup	GRCh38
NC_000011.9:g.20804920dup , CM000673.1:g.20804920dup	GRCh37
NC_000011.8:g.20761496dup	NCBI36
NG_047064.1:g.118824dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.185-306dup MANE Select	ENSP00000349654.5:n.185-306dup
ENST00000298925.9:c.269-306dup	ENSP00000298925.5:n.269-306dup
ENST00000325319.9:c.185-306dup	ENSP00000317837.5:n.185-306dup
ENST00000357134.9:c.185-306dup	ENSP00000349654.5:n.185-306dup
ENST00000527873.5:n.206-306dup
ENST00000528046.5:n.368-306dup
ENST00000529595.1:n.73-306dup
ENST00000532434.5:c.185-306dup	ENSP00000437170.1:n.185-306dup
ENST00000619031.4:c.-528-306dup	ENSP00000479479.1:n.-528-306dup
NM_001288713.1:c.269-306dup	NP_001275642.1:n.269-306dup
NM_001288714.1:c.185-306dup	NP_001275643.1:n.185-306dup
NM_006157.4:c.185-306dup	NP_006148.2:n.185-306dup
NM_201551.2:c.185-306dup	NP_963845.1:n.185-306dup
NM_006157.5:c.185-306dup MANE Select	NP_006148.2:n.185-306dup