Canonical Allele Identifier: CA2693514079
Gene: NDP HGNC NCBI

Linked Data

gnomAD v4: X-43949465-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949465C>T , CM000685.2:g.43949465C>T GRCh38
NC_000023.10:g.43808711C>T , CM000685.1:g.43808711C>T GRCh37
NC_000023.9:g.43693655C>T NCBI36
NG_009832.1:g.29211G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*334G>A MANE Select ENSP00000495972.1:n.*334G>A
ENST00000647044.1:c.*334G>A ENSP00000495811.1:n.*334G>A
ENST00000378062.5:c.*334G>A ENSP00000367301.5:n.*334G>A
NM_000266.3:c.*334G>A NP_000257.1:n.*334G>A
NM_000266.4:c.*334G>A MANE Select NP_000257.1:n.*334G>A
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