Canonical Allele Identifier: CA1957063703
Gene: NELL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.21543535G= , CM000673.2:g.21543535G= GRCh38
NC_000011.9:g.21565081G= , CM000673.1:g.21565081G= GRCh37
NC_000011.8:g.21521657G= NCBI36
NG_047064.1:g.878985G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357134.10:c.1786+9021G= MANE Select ENSP00000349654.5:n.1786+9021G=
ENST00000298925.9:c.1870+9021G= ENSP00000298925.5:n.1870+9021G=
ENST00000325319.9:c.1615+9021G= ENSP00000317837.5:n.1615+9021G=
ENST00000357134.9:c.1786+9021G= ENSP00000349654.5:n.1786+9021G=
ENST00000529218.5:n.1140+9021G=
ENST00000532434.5:c.1646-16654G= ENSP00000437170.1:n.1646-16654G=
ENST00000619031.4:c.1066+9021G= ENSP00000479479.1:n.1066+9021G=
NM_001288713.1:c.1870+9021G= NP_001275642.1:n.1870+9021G=
NM_001288714.1:c.1615+9021G= NP_001275643.1:n.1615+9021G=
NM_006157.4:c.1786+9021G= NP_006148.2:n.1786+9021G=
NM_201551.2:c.1646-16654G= NP_963845.1:n.1646-16654G=
XM_011520119.1:c.829+9021G= XP_011518421.1:n.829+9021G=
NM_006157.5:c.1786+9021G= MANE Select NP_006148.2:n.1786+9021G=