Canonical Allele Identifier: CA2426745192
Gene: NDP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949688G= , CM000685.2:g.43949688G= GRCh38
NC_000023.10:g.43808934G= , CM000685.1:g.43808934G= GRCh37
NC_000023.9:g.43693878G= NCBI36
NG_009832.1:g.28988C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*111C= MANE Select ENSP00000495972.1:n.*111C=
ENST00000647044.1:c.*111C= ENSP00000495811.1:n.*111C=
ENST00000378062.5:c.*111C= ENSP00000367301.5:n.*111C=
ENST00000470584.1:n.557C=
NM_000266.3:c.*111C= NP_000257.1:n.*111C=
NM_000266.4:c.*111C= MANE Select NP_000257.1:n.*111C=