Canonical Allele Identifier: CA2693514119
Gene: NDP HGNC NCBI

Linked Data

gnomAD v4: X-43949564-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949564T>C , CM000685.2:g.43949564T>C GRCh38
NC_000023.10:g.43808810T>C , CM000685.1:g.43808810T>C GRCh37
NC_000023.9:g.43693754T>C NCBI36
NG_009832.1:g.29112A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*235A>G MANE Select ENSP00000495972.1:n.*235A>G
ENST00000647044.1:c.*235A>G ENSP00000495811.1:n.*235A>G
ENST00000378062.5:c.*235A>G ENSP00000367301.5:n.*235A>G
NM_000266.3:c.*235A>G NP_000257.1:n.*235A>G
NM_000266.4:c.*235A>G MANE Select NP_000257.1:n.*235A>G
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