Canonical Allele Identifier: CA218895446

Gene: NELL1

Linked Data

• dbSNP Id: rs1491166705
• MyVariant Identifiers: chr11:g.20804920_20804921del (hg19) ; chr11:g.20783374_20783375del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783375_20783376del , CM000673.2:g.20783375_20783376del	GRCh38
NC_000011.9:g.20804921_20804922del , CM000673.1:g.20804921_20804922del	GRCh37
NC_000011.8:g.20761497_20761498del	NCBI36
NG_047064.1:g.118825_118826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.185-305_185-304del MANE Select	ENSP00000349654.5:n.185-305_185-304del
ENST00000298925.9:c.269-305_269-304del	ENSP00000298925.5:n.269-305_269-304del
ENST00000325319.9:c.185-305_185-304del	ENSP00000317837.5:n.185-305_185-304del
ENST00000357134.9:c.185-305_185-304del	ENSP00000349654.5:n.185-305_185-304del
ENST00000527873.5:n.206-305_206-304del
ENST00000528046.5:n.368-305_368-304del
ENST00000529595.1:n.73-305_73-304del
ENST00000532434.5:c.185-305_185-304del	ENSP00000437170.1:n.185-305_185-304del
ENST00000619031.4:c.-528-305_-528-304del	ENSP00000479479.1:n.-528-305_-528-304del
NM_001288713.1:c.269-305_269-304del	NP_001275642.1:n.269-305_269-304del
NM_001288714.1:c.185-305_185-304del	NP_001275643.1:n.185-305_185-304del
NM_006157.4:c.185-305_185-304del	NP_006148.2:n.185-305_185-304del
NM_201551.2:c.185-305_185-304del	NP_963845.1:n.185-305_185-304del
NM_006157.5:c.185-305_185-304del MANE Select	NP_006148.2:n.185-305_185-304del