Canonical Allele Identifier: CA2612834582

Gene: NELL1

Linked Data

• gnomAD v4: 11-20783812-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783812_20783813insG , CM000673.2:g.20783812_20783813insG	GRCh38
NC_000011.9:g.20805358_20805359insG , CM000673.1:g.20805358_20805359insG	GRCh37
NC_000011.8:g.20761934_20761935insG	NCBI36
NG_047064.1:g.119262_119263insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.317_318insG MANE Select	ENSP00000349654.5:p.Ile106MetfsTer10
ENST00000298925.9:c.401_402insG	ENSP00000298925.5:p.Ile134MetfsTer10
ENST00000325319.9:c.317_318insG	ENSP00000317837.5:p.Ile106MetfsTer10
ENST00000357134.9:c.317_318insG	ENSP00000349654.5:p.Ile106MetfsTer10
ENST00000524738.1:n.144_145insG
ENST00000527873.5:n.338_339insG
ENST00000528046.5:n.500_501insG
ENST00000529595.1:n.205_206insG
ENST00000532434.5:c.317_318insG	ENSP00000437170.1:p.Ile106MetfsTer10
ENST00000619031.4:c.-396_-395insG	ENSP00000479479.1:n.-396_-395insG
NM_001288713.1:c.401_402insG	NP_001275642.1:p.Ile134MetfsTer10
NM_001288714.1:c.317_318insG	NP_001275643.1:p.Ile106MetfsTer10
NM_006157.4:c.317_318insG	NP_006148.2:p.Ile106MetfsTer10
NM_201551.2:c.317_318insG	NP_963845.1:p.Ile106MetfsTer10
NM_006157.5:c.317_318insG MANE Select	NP_006148.2:p.Ile106MetfsTer10