Canonical Allele Identifier: CA2579590497
Gene: NDP HGNC NCBI

Linked Data

gnomAD v4: X-43949730-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949730A>G , CM000685.2:g.43949730A>G GRCh38
NC_000023.10:g.43808976A>G , CM000685.1:g.43808976A>G GRCh37
NC_000023.9:g.43693920A>G NCBI36
NG_009832.1:g.28946T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*69T>C MANE Select ENSP00000495972.1:n.*69T>C
ENST00000647044.1:c.*69T>C ENSP00000495811.1:n.*69T>C
ENST00000378062.5:c.*69T>C ENSP00000367301.5:n.*69T>C
ENST00000470584.1:n.515T>C
NM_000266.3:c.*69T>C NP_000257.1:n.*69T>C
NM_000266.4:c.*69T>C MANE Select NP_000257.1:n.*69T>C
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