Canonical Allele Identifier: CA2426745141
Gene: NDP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949508C= , CM000685.2:g.43949508C= GRCh38
NC_000023.10:g.43808754C= , CM000685.1:g.43808754C= GRCh37
NC_000023.9:g.43693698C= NCBI36
NG_009832.1:g.29168G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*291G= MANE Select ENSP00000495972.1:n.*291G=
ENST00000647044.1:c.*291G= ENSP00000495811.1:n.*291G=
ENST00000378062.5:c.*291G= ENSP00000367301.5:n.*291G=
NM_000266.3:c.*291G= NP_000257.1:n.*291G=
NM_000266.4:c.*291G= MANE Select NP_000257.1:n.*291G=