Canonical Allele Identifier: CA2426745133
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs2035747672
gnomAD v4: X-43949490-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949490C>A , CM000685.2:g.43949490C>A GRCh38
NC_000023.10:g.43808736C>A , CM000685.1:g.43808736C>A GRCh37
NC_000023.9:g.43693680C>A NCBI36
NG_009832.1:g.29186G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*309G>T MANE Select ENSP00000495972.1:n.*309G>T
ENST00000647044.1:c.*309G>T ENSP00000495811.1:n.*309G>T
ENST00000378062.5:c.*309G>T ENSP00000367301.5:n.*309G>T
NM_000266.3:c.*309G>T NP_000257.1:n.*309G>T
NM_000266.4:c.*309G>T MANE Select NP_000257.1:n.*309G>T