Canonical Allele Identifier: CA2426745182
Gene: NDP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949654A= , CM000685.2:g.43949654A= GRCh38
NC_000023.10:g.43808900A= , CM000685.1:g.43808900A= GRCh37
NC_000023.9:g.43693844A= NCBI36
NG_009832.1:g.29022T=

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*145T= MANE Select ENSP00000495972.1:n.*145T=
ENST00000647044.1:c.*145T= ENSP00000495811.1:n.*145T=
ENST00000378062.5:c.*145T= ENSP00000367301.5:n.*145T=
NM_000266.3:c.*145T= NP_000257.1:n.*145T=
NM_000266.4:c.*145T= MANE Select NP_000257.1:n.*145T=
Search 100 bp 5'
Search 100 bp 3'