Canonical Allele Identifier: CA2693514092
Gene: NDP HGNC NCBI

Linked Data

gnomAD v4: X-43949492-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949497del , CM000685.2:g.43949497del GRCh38
NC_000023.10:g.43808743del , CM000685.1:g.43808743del GRCh37
NC_000023.9:g.43693687del NCBI36
NG_009832.1:g.29183del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*306del MANE Select ENSP00000495972.1:n.*306del
ENST00000647044.1:c.*306del ENSP00000495811.1:n.*306del
ENST00000378062.5:c.*306del ENSP00000367301.5:n.*306del
NM_000266.3:c.*306del NP_000257.1:n.*306del
NM_000266.4:c.*306del MANE Select NP_000257.1:n.*306del
Search 100 bp 5'
Search 100 bp 3'