Canonical Allele Identifier: CA2693514178
Gene: NDP HGNC NCBI

Linked Data

gnomAD v4: X-43949682-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949682T>A , CM000685.2:g.43949682T>A GRCh38
NC_000023.10:g.43808928T>A , CM000685.1:g.43808928T>A GRCh37
NC_000023.9:g.43693872T>A NCBI36
NG_009832.1:g.28994A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*117A>T MANE Select ENSP00000495972.1:n.*117A>T
ENST00000647044.1:c.*117A>T ENSP00000495811.1:n.*117A>T
ENST00000378062.5:c.*117A>T ENSP00000367301.5:n.*117A>T
ENST00000470584.1:n.563A>T
NM_000266.3:c.*117A>T NP_000257.1:n.*117A>T
NM_000266.4:c.*117A>T MANE Select NP_000257.1:n.*117A>T