Canonical Allele Identifier: CA218895448

Gene: NELL1

Linked Data

• MyVariant Identifiers: chr11:g.20804920_20804921insTC (hg19) ; chr11:g.20783374_20783375insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783374_20783375insTC , CM000673.2:g.20783374_20783375insTC	GRCh38
NC_000011.9:g.20804920_20804921insTC , CM000673.1:g.20804920_20804921insTC	GRCh37
NC_000011.8:g.20761496_20761497insTC	NCBI36
NG_047064.1:g.118824_118825insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.185-306_185-305insTC MANE Select	ENSP00000349654.5:n.185-306_185-305insTC
ENST00000298925.9:c.269-306_269-305insTC	ENSP00000298925.5:n.269-306_269-305insTC
ENST00000325319.9:c.185-306_185-305insTC	ENSP00000317837.5:n.185-306_185-305insTC
ENST00000357134.9:c.185-306_185-305insTC	ENSP00000349654.5:n.185-306_185-305insTC
ENST00000527873.5:n.206-306_206-305insTC
ENST00000528046.5:n.368-306_368-305insTC
ENST00000529595.1:n.73-306_73-305insTC
ENST00000532434.5:c.185-306_185-305insTC	ENSP00000437170.1:n.185-306_185-305insTC
ENST00000619031.4:c.-528-306_-528-305insTC	ENSP00000479479.1:n.-528-306_-528-305insTC
NM_001288713.1:c.269-306_269-305insTC	NP_001275642.1:n.269-306_269-305insTC
NM_001288714.1:c.185-306_185-305insTC	NP_001275643.1:n.185-306_185-305insTC
NM_006157.4:c.185-306_185-305insTC	NP_006148.2:n.185-306_185-305insTC
NM_201551.2:c.185-306_185-305insTC	NP_963845.1:n.185-306_185-305insTC
NM_006157.5:c.185-306_185-305insTC MANE Select	NP_006148.2:n.185-306_185-305insTC