Canonical Allele Identifier: CA473461458

Gene: NELL1

Linked Data

• dbSNP Id: rs1856898544
• COSMIC: COSM5647804
• MyVariant Identifiers: chr11:g.20805305C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783759C>A , CM000673.2:g.20783759C>A	GRCh38
NC_000011.9:g.20805305C>A , CM000673.1:g.20805305C>A	GRCh37
NC_000011.8:g.20761881C>A	NCBI36
NG_047064.1:g.119209C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.264C>A MANE Select	ENSP00000349654.5:p.Thr88=
ENST00000298925.9:c.348C>A	ENSP00000298925.5:p.Thr116=
ENST00000325319.9:c.264C>A	ENSP00000317837.5:p.Thr88=
ENST00000357134.9:c.264C>A	ENSP00000349654.5:p.Thr88=
ENST00000524738.1:n.91C>A
ENST00000527873.5:n.285C>A
ENST00000528046.5:n.447C>A
ENST00000529595.1:n.152C>A
ENST00000532434.5:c.264C>A	ENSP00000437170.1:p.Thr88=
ENST00000619031.4:c.-449C>A	ENSP00000479479.1:n.-449C>A
NM_001288713.1:c.348C>A	NP_001275642.1:p.Thr116=
NM_001288714.1:c.264C>A	NP_001275643.1:p.Thr88=
NM_006157.4:c.264C>A	NP_006148.2:p.Thr88=
NM_201551.2:c.264C>A	NP_963845.1:p.Thr88=
NM_006157.5:c.264C>A MANE Select	NP_006148.2:p.Thr88=