Canonical Allele Identifier: CA2612834428

Gene: NELL1

Linked Data

• gnomAD v4: 11-20783554-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783554A>C , CM000673.2:g.20783554A>C	GRCh38
NC_000011.9:g.20805100A>C , CM000673.1:g.20805100A>C	GRCh37
NC_000011.8:g.20761676A>C	NCBI36
NG_047064.1:g.119004A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.185-126A>C MANE Select	ENSP00000349654.5:n.185-126A>C
ENST00000298925.9:c.269-126A>C	ENSP00000298925.5:n.269-126A>C
ENST00000325319.9:c.185-126A>C	ENSP00000317837.5:n.185-126A>C
ENST00000357134.9:c.185-126A>C	ENSP00000349654.5:n.185-126A>C
ENST00000527873.5:n.206-126A>C
ENST00000528046.5:n.368-126A>C
ENST00000529595.1:n.73-126A>C
ENST00000532434.5:c.185-126A>C	ENSP00000437170.1:n.185-126A>C
ENST00000619031.4:c.-528-126A>C	ENSP00000479479.1:n.-528-126A>C
NM_001288713.1:c.269-126A>C	NP_001275642.1:n.269-126A>C
NM_001288714.1:c.185-126A>C	NP_001275643.1:n.185-126A>C
NM_006157.4:c.185-126A>C	NP_006148.2:n.185-126A>C
NM_201551.2:c.185-126A>C	NP_963845.1:n.185-126A>C
NM_006157.5:c.185-126A>C MANE Select	NP_006148.2:n.185-126A>C