Canonical Allele Identifier: CA12262141
Gene: NEDD9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11310186C>T , CM000668.2:g.11310186C>T GRCh38
NC_000006.11:g.11310419C>T , CM000668.1:g.11310419C>T GRCh37
NC_000006.10:g.11418405C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397378.7:c.-152-4031G>A ENSP00000380534.3:n.-152-4031G>A
ENST00000448183.6:c.-152-4031G>A ENSP00000395237.2:n.-152-4031G>A
ENST00000459670.2:n.169-4031G>A
ENST00000468612.5:n.201-4031G>A
ENST00000504387.5:c.-152-4031G>A ENSP00000422871.1:n.-152-4031G>A
ENST00000504634.5:n.195-4031G>A
ENST00000508546.5:c.-343-4031G>A ENSP00000424975.1:n.-343-4031G>A
ENST00000512665.5:n.135-4031G>A
ENST00000513989.5:c.-333-4031G>A ENSP00000421282.1:n.-333-4031G>A
ENST00000514660.1:n.171-4031G>A
NM_001142393.1:c.-152-4031G>A NP_001135865.1:n.-152-4031G>A
NR_073131.1:n.211-4031G>A
XR_926469.1:n.842+4004C>T
XR_926470.1:n.489+4004C>T
XR_926471.1:n.842+4004C>T
XR_926472.1:n.845+4004C>T
XR_926473.1:n.992+567C>T
XR_926474.1:n.842+4004C>T
XR_926475.1:n.710+4004C>T
XR_001743962.1:n.465+4004C>T
XR_001743963.1:n.484+4004C>T
XR_001743965.1:n.465+4004C>T
XR_001743966.1:n.465+4004C>T
XR_001743967.1:n.465+4004C>T
XR_926469.2:n.871+4004C>T
XR_926470.2:n.489+4004C>T
NM_001142393.2:c.-152-4031G>A NP_001135865.1:n.-152-4031G>A
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