Canonical Allele Identifier: CA817390341

Gene: NEDD9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11334421C>T , CM000668.2:g.11334421C>T	GRCh38
NC_000006.11:g.11334654C>T , CM000668.1:g.11334654C>T	GRCh37
NC_000006.10:g.11442640C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397378.7:c.-153+80G>A	ENSP00000380534.3:n.-153+80G>A
ENST00000448183.6:c.-152-28266G>A	ENSP00000395237.2:n.-152-28266G>A
ENST00000459670.2:n.169-28266G>A
ENST00000461055.2:n.241+80G>A
ENST00000468612.5:n.201-28266G>A
ENST00000504387.5:c.-152-28266G>A	ENSP00000422871.1:n.-152-28266G>A
ENST00000504634.5:n.195-28266G>A
ENST00000508546.5:c.-343-28266G>A	ENSP00000424975.1:n.-343-28266G>A
ENST00000512665.5:n.135-28266G>A
ENST00000513989.5:c.-333-28266G>A	ENSP00000421282.1:n.-333-28266G>A
ENST00000514660.1:n.171-28266G>A
NM_001142393.1:c.-152-28266G>A	NP_001135865.1:n.-152-28266G>A
NR_073131.1:n.211-28266G>A
XR_926474.1:n.1220-325C>T
XR_001743967.1:n.843-325C>T
NM_001142393.2:c.-152-28266G>A	NP_001135865.1:n.-152-28266G>A