Canonical Allele Identifier: CA2693514066

Gene: NDP

Linked Data

• gnomAD v4: X-43949441-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43949441C>A , CM000685.2:g.43949441C>A	GRCh38
NC_000023.10:g.43808687C>A , CM000685.1:g.43808687C>A	GRCh37
NC_000023.9:g.43693631C>A	NCBI36
NG_009832.1:g.29235G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642620.1:c.*358G>T MANE Select	ENSP00000495972.1:n.*358G>T
ENST00000647044.1:c.*358G>T	ENSP00000495811.1:n.*358G>T
ENST00000378062.5:c.*358G>T	ENSP00000367301.5:n.*358G>T
NM_000266.3:c.*358G>T	NP_000257.1:n.*358G>T
NM_000266.4:c.*358G>T MANE Select	NP_000257.1:n.*358G>T