Canonical Allele Identifier: CA875556710
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs1193912853
MyVariant Identifiers: chrX:g.43808791_43808792insGGGGAAAATGCCTGA (hg19) chrX:g.43949545_43949546insGGGGAAAATGCCTGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949546_43949560dup , CM000685.2:g.43949546_43949560dup GRCh38
NC_000023.10:g.43808792_43808806dup , CM000685.1:g.43808792_43808806dup GRCh37
NC_000023.9:g.43693736_43693750dup NCBI36
NG_009832.1:g.29116_29130dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*239_*253dup MANE Select ENSP00000495972.1:n.*239_*253dup
ENST00000647044.1:c.*239_*253dup ENSP00000495811.1:n.*239_*253dup
ENST00000378062.5:c.*239_*253dup ENSP00000367301.5:n.*239_*253dup
NM_000266.3:c.*239_*253dup NP_000257.1:n.*239_*253dup
NM_000266.4:c.*239_*253dup MANE Select NP_000257.1:n.*239_*253dup
Search 100 bp 5'
Search 100 bp 3'