Canonical Allele Identifier: CA2426745143
Gene: NDP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949513T= , CM000685.2:g.43949513T= GRCh38
NC_000023.10:g.43808759T= , CM000685.1:g.43808759T= GRCh37
NC_000023.9:g.43693703T= NCBI36
NG_009832.1:g.29163A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*286A= MANE Select ENSP00000495972.1:n.*286A=
ENST00000647044.1:c.*286A= ENSP00000495811.1:n.*286A=
ENST00000378062.5:c.*286A= ENSP00000367301.5:n.*286A=
NM_000266.3:c.*286A= NP_000257.1:n.*286A=
NM_000266.4:c.*286A= MANE Select NP_000257.1:n.*286A=
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