Canonical Allele Identifier: CA270855987

Gene: NEDD4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55918731A>G , CM000677.2:g.55918731A>G	GRCh38
NC_000015.9:g.56210929A>G , CM000677.1:g.56210929A>G	GRCh37
NC_000015.8:g.53998221A>G	NCBI36
NG_051072.1:g.80016T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435532.8:c.291+5915T>C MANE Select	ENSP00000410613.3:n.291+5915T>C
ENST00000648451.1:c.*70+5915T>C	ENSP00000498181.1:n.*70+5915T>C
ENST00000435532.7:c.291+5915T>C	ENSP00000410613.3:n.291+5915T>C
ENST00000502612.5:c.205+5915T>C
ENST00000507063.1:c.79+5915T>C
ENST00000514893.5:n.264+5915T>C
NM_006154.3:c.291+5915T>C	NP_006145.2:n.291+5915T>C
XM_011521624.1:c.216+5915T>C	XP_011519926.1:n.216+5915T>C
XM_011521625.1:c.138+5915T>C	XP_011519927.1:n.138+5915T>C
XM_011521626.1:c.138+5915T>C	XP_011519928.1:n.138+5915T>C
XM_011521627.1:c.72+5915T>C	XP_011519929.1:n.72+5915T>C
NM_001329212.1:c.-151+5915T>C	NP_001316141.1:n.-151+5915T>C
XM_011521624.3:c.216+5915T>C	XP_011519926.1:n.216+5915T>C
XM_011521625.3:c.138+5915T>C	XP_011519927.1:n.138+5915T>C
NM_001329212.2:c.-151+5915T>C	NP_001316141.1:n.-151+5915T>C
NM_006154.4:c.291+5915T>C MANE Select	NP_006145.2:n.291+5915T>C