Canonical Allele Identifier: CA2693514180
Gene: NDP HGNC NCBI

Linked Data

gnomAD v4: X-43949685-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949685C>A , CM000685.2:g.43949685C>A GRCh38
NC_000023.10:g.43808931C>A , CM000685.1:g.43808931C>A GRCh37
NC_000023.9:g.43693875C>A NCBI36
NG_009832.1:g.28991G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*114G>T MANE Select ENSP00000495972.1:n.*114G>T
ENST00000647044.1:c.*114G>T ENSP00000495811.1:n.*114G>T
ENST00000378062.5:c.*114G>T ENSP00000367301.5:n.*114G>T
ENST00000470584.1:n.560G>T
NM_000266.3:c.*114G>T NP_000257.1:n.*114G>T
NM_000266.4:c.*114G>T MANE Select NP_000257.1:n.*114G>T
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