Canonical Allele Identifier: CA1956698018

Gene: NELL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783768C= , CM000673.2:g.20783768C=	GRCh38
NC_000011.9:g.20805314C= , CM000673.1:g.20805314C=	GRCh37
NC_000011.8:g.20761890C=	NCBI36
NG_047064.1:g.119218C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.273C= MANE Select	ENSP00000349654.5:p.Ala91=
ENST00000298925.9:c.357C=	ENSP00000298925.5:p.Ala119=
ENST00000325319.9:c.273C=	ENSP00000317837.5:p.Ala91=
ENST00000357134.9:c.273C=	ENSP00000349654.5:p.Ala91=
ENST00000524738.1:n.100C=
ENST00000527873.5:n.294C=
ENST00000528046.5:n.456C=
ENST00000529595.1:n.161C=
ENST00000532434.5:c.273C=	ENSP00000437170.1:p.Ala91=
ENST00000619031.4:c.-440C=	ENSP00000479479.1:n.-440C=
NM_001288713.1:c.357C=	NP_001275642.1:p.Ala119=
NM_001288714.1:c.273C=	NP_001275643.1:p.Ala91=
NM_006157.4:c.273C=	NP_006148.2:p.Ala91=
NM_201551.2:c.273C=	NP_963845.1:p.Ala91=
NM_006157.5:c.273C= MANE Select	NP_006148.2:p.Ala91=