Canonical Allele Identifier: CA12383810
Gene: NEDD9 HGNC NCBI

Linked Data

dbSNP Id: rs11961171
gnomAD v2: 6-11276028-G-A
gnomAD v3: 6-11275795-G-A
gnomAD v4: 6-11275795-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11275795G>A , CM000668.2:g.11275795G>A GRCh38
NC_000006.11:g.11276028G>A , CM000668.1:g.11276028G>A GRCh37
NC_000006.10:g.11384014G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000397378.7:c.12+30197C>T ENSP00000380534.3:n.12+30197C>T
ENST00000448183.6:c.106+29271C>T ENSP00000395237.2:n.106+29271C>T
ENST00000468612.5:n.365-24069C>T
ENST00000504387.5:c.12+30197C>T ENSP00000422871.1:n.12+30197C>T
ENST00000504634.5:n.359-3963C>T
ENST00000508546.5:c.-179-24069C>T ENSP00000424975.1:n.-179-24069C>T
ENST00000512665.5:n.299-24069C>T
ENST00000513989.5:c.-169-24069C>T ENSP00000421282.1:n.-169-24069C>T
NM_001142393.1:c.12+30197C>T NP_001135865.1:n.12+30197C>T
NR_073131.1:n.468+29271C>T
NM_001142393.2:c.12+30197C>T NP_001135865.1:n.12+30197C>T