Canonical Allele Identifier: CA2693514078
Gene: NDP HGNC NCBI

Linked Data

gnomAD v4: X-43949463-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949463A>G , CM000685.2:g.43949463A>G GRCh38
NC_000023.10:g.43808709A>G , CM000685.1:g.43808709A>G GRCh37
NC_000023.9:g.43693653A>G NCBI36
NG_009832.1:g.29213T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*336T>C MANE Select ENSP00000495972.1:n.*336T>C
ENST00000647044.1:c.*336T>C ENSP00000495811.1:n.*336T>C
ENST00000378062.5:c.*336T>C ENSP00000367301.5:n.*336T>C
NM_000266.3:c.*336T>C NP_000257.1:n.*336T>C
NM_000266.4:c.*336T>C MANE Select NP_000257.1:n.*336T>C