Canonical Allele Identifier: CA14178251

Gene: NEDD4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55902679T>C , CM000677.2:g.55902679T>C	GRCh38
NC_000015.9:g.56194877T>C , CM000677.1:g.56194877T>C	GRCh37
NC_000015.8:g.53982169T>C	NCBI36
NG_051072.1:g.96068A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435532.8:c.291+21967A>G MANE Select	ENSP00000410613.3:n.291+21967A>G
ENST00000648451.1:c.*70+21967A>G	ENSP00000498181.1:n.*70+21967A>G
ENST00000338963.6:c.1548+12605A>G	ENSP00000345530.2:n.1548+12605A>G
ENST00000435532.7:c.291+21967A>G	ENSP00000410613.3:n.291+21967A>G
ENST00000502612.5:c.205+21967A>G
ENST00000503468.5:c.1186+12605A>G
ENST00000506154.1:c.1548+12605A>G	ENSP00000422705.1:n.1548+12605A>G
ENST00000507063.1:c.149+2533A>G
ENST00000508342.5:c.1548+12605A>G	ENSP00000424827.1:n.1548+12605A>G
ENST00000508871.5:c.371+12605A>G
ENST00000514893.5:n.264+21967A>G
NM_001284338.1:c.1548+12605A>G	NP_001271267.1:n.1548+12605A>G
NM_001284339.1:c.1548+12605A>G	NP_001271268.1:n.1548+12605A>G
NM_001284340.1:c.1548+12605A>G	NP_001271269.1:n.1548+12605A>G
NM_006154.3:c.291+21967A>G	NP_006145.2:n.291+21967A>G
NM_198400.3:c.1548+12605A>G	NP_940682.2:n.1548+12605A>G
NR_104302.1:n.1848+12605A>G
XM_011521624.1:c.216+21967A>G	XP_011519926.1:n.216+21967A>G
XM_011521625.1:c.138+21967A>G	XP_011519927.1:n.138+21967A>G
XM_011521626.1:c.138+21967A>G	XP_011519928.1:n.138+21967A>G
XM_011521627.1:c.72+21967A>G	XP_011519929.1:n.72+21967A>G
NM_001329212.1:c.-151+21967A>G	NP_001316141.1:n.-151+21967A>G
XM_011521624.3:c.216+21967A>G	XP_011519926.1:n.216+21967A>G
XM_011521625.3:c.138+21967A>G	XP_011519927.1:n.138+21967A>G
NM_001329212.2:c.-151+21967A>G	NP_001316141.1:n.-151+21967A>G
NM_006154.4:c.291+21967A>G MANE Select	NP_006145.2:n.291+21967A>G
NM_001284338.2:c.1548+12605A>G	NP_001271267.1:n.1548+12605A>G
NR_104302.2:n.1853+12605A>G