Canonical Allele Identifier: CA329483944
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs765315655
gnomAD v2: X-43808714-GAC-G
gnomAD v3: X-43949468-GAC-G
gnomAD v4: X-43949468-GAC-G
MyVariant Identifiers: chrX:g.43808715_43808716del (hg19) chrX:g.43949469_43949470del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949471_43949472del , CM000685.2:g.43949471_43949472del GRCh38
NC_000023.10:g.43808717_43808718del , CM000685.1:g.43808717_43808718del GRCh37
NC_000023.9:g.43693661_43693662del NCBI36
NG_009832.1:g.29206_29207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*329_*330del MANE Select ENSP00000495972.1:n.*329_*330del
ENST00000647044.1:c.*329_*330del ENSP00000495811.1:n.*329_*330del
ENST00000378062.5:c.*329_*330del ENSP00000367301.5:n.*329_*330del
NM_000266.3:c.*329_*330del NP_000257.1:n.*329_*330del
NM_000266.4:c.*329_*330del MANE Select NP_000257.1:n.*329_*330del
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