Canonical Allele Identifier: CA1132659298
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs2035747962
gnomAD v3: X-43949515-G-A
gnomAD v4: X-43949515-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949515G>A , CM000685.2:g.43949515G>A GRCh38
NC_000023.10:g.43808761G>A , CM000685.1:g.43808761G>A GRCh37
NC_000023.9:g.43693705G>A NCBI36
NG_009832.1:g.29161C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*284C>T MANE Select ENSP00000495972.1:n.*284C>T
ENST00000647044.1:c.*284C>T ENSP00000495811.1:n.*284C>T
ENST00000378062.5:c.*284C>T ENSP00000367301.5:n.*284C>T
NM_000266.3:c.*284C>T NP_000257.1:n.*284C>T
NM_000266.4:c.*284C>T MANE Select NP_000257.1:n.*284C>T
Search 100 bp 5'
Search 100 bp 3'