Canonical Allele Identifier: CA641904879
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs1196140316

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949656_43949657del , CM000685.2:g.43949656_43949657del GRCh38
NC_000023.10:g.43808902_43808903del , CM000685.1:g.43808902_43808903del GRCh37
NC_000023.9:g.43693846_43693847del NCBI36
NG_009832.1:g.29021_29022del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*144_*145del MANE Select ENSP00000495972.1:n.*144_*145del
ENST00000647044.1:c.*144_*145del ENSP00000495811.1:n.*144_*145del
ENST00000378062.5:c.*144_*145del ENSP00000367301.5:n.*144_*145del
NM_000266.3:c.*144_*145del NP_000257.1:n.*144_*145del
NM_000266.4:c.*144_*145del MANE Select NP_000257.1:n.*144_*145del