Canonical Allele Identifier: CA875556747
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs1412341294
gnomAD v4: X-43949688-G-C
MyVariant Identifiers: chrX:g.43808934G>C (hg19) chrX:g.43949688G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949688G>C , CM000685.2:g.43949688G>C GRCh38
NC_000023.10:g.43808934G>C , CM000685.1:g.43808934G>C GRCh37
NC_000023.9:g.43693878G>C NCBI36
NG_009832.1:g.28988C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*111C>G MANE Select ENSP00000495972.1:n.*111C>G
ENST00000647044.1:c.*111C>G ENSP00000495811.1:n.*111C>G
ENST00000378062.5:c.*111C>G ENSP00000367301.5:n.*111C>G
ENST00000470584.1:n.557C>G
NM_000266.3:c.*111C>G NP_000257.1:n.*111C>G
NM_000266.4:c.*111C>G MANE Select NP_000257.1:n.*111C>G
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