Canonical Allele Identifier: CA2820657031
Gene: NDP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949535_43949536del , CM000685.2:g.43949535_43949536del GRCh38
NC_000023.10:g.43808781_43808782del , CM000685.1:g.43808781_43808782del GRCh37
NC_000023.9:g.43693725_43693726del NCBI36
NG_009832.1:g.29140_29141del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*263_*264del MANE Select ENSP00000495972.1:n.*263_*264del
ENST00000647044.1:c.*263_*264del ENSP00000495811.1:n.*263_*264del
ENST00000378062.5:c.*263_*264del ENSP00000367301.5:n.*263_*264del
NM_000266.3:c.*263_*264del NP_000257.1:n.*263_*264del
NM_000266.4:c.*263_*264del MANE Select NP_000257.1:n.*263_*264del