Canonical Allele Identifier: CA413007572
Gene: NDP HGNC NCBI
NDP-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1678208
ClinVar RCV Id: RCV002224799
dbSNP Id: rs2147204773
MyVariant Identifiers: chrX:g.43809170A>G (hg19) chrX:g.43949924A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949924A>G , CM000685.2:g.43949924A>G GRCh38
NC_000023.10:g.43809170A>G , CM000685.1:g.43809170A>G GRCh37
NC_000023.9:g.43694114A>G NCBI36
NG_009832.1:g.28752T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.277T>C (NDP) MANE Select ENSP00000495972.1:p.Cys93Arg
ENST00000647044.1:c.277T>C (NDP) ENSP00000495811.1:p.Cys93Arg
ENST00000378062.5:c.277T>C (NDP) ENSP00000367301.5:p.Cys93Arg
ENST00000470584.1:n.321T>C (NDP)
NM_000266.3:c.277T>C (NDP) NP_000257.1:p.Cys93Arg
NR_046631.1:n.193A>G (NDP-AS1)
NM_000266.4:c.277T>C (NDP) MANE Select NP_000257.1:p.Cys93Arg
Search 100 bp 5'
Search 100 bp 3'