Canonical Allele Identifier: CA329483953
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs900452652
gnomAD v4: X-43949533-A-G
MyVariant Identifiers: chrX:g.43808779A>G (hg19) chrX:g.43949533A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949533A>G , CM000685.2:g.43949533A>G GRCh38
NC_000023.10:g.43808779A>G , CM000685.1:g.43808779A>G GRCh37
NC_000023.9:g.43693723A>G NCBI36
NG_009832.1:g.29143T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*266T>C MANE Select ENSP00000495972.1:n.*266T>C
ENST00000647044.1:c.*266T>C ENSP00000495811.1:n.*266T>C
ENST00000378062.5:c.*266T>C ENSP00000367301.5:n.*266T>C
NM_000266.3:c.*266T>C NP_000257.1:n.*266T>C
NM_000266.4:c.*266T>C MANE Select NP_000257.1:n.*266T>C
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