Canonical Allele Identifier: CA2820657029
Gene: NDP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949497T>C , CM000685.2:g.43949497T>C GRCh38
NC_000023.10:g.43808743T>C , CM000685.1:g.43808743T>C GRCh37
NC_000023.9:g.43693687T>C NCBI36
NG_009832.1:g.29179A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*302A>G MANE Select ENSP00000495972.1:n.*302A>G
ENST00000647044.1:c.*302A>G ENSP00000495811.1:n.*302A>G
ENST00000378062.5:c.*302A>G ENSP00000367301.5:n.*302A>G
NM_000266.3:c.*302A>G NP_000257.1:n.*302A>G
NM_000266.4:c.*302A>G MANE Select NP_000257.1:n.*302A>G