Canonical Allele Identifier: CA2693514101

Gene: NDP

Linked Data

• gnomAD v4: X-43949531-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43949531G>A , CM000685.2:g.43949531G>A	GRCh38
NC_000023.10:g.43808777G>A , CM000685.1:g.43808777G>A	GRCh37
NC_000023.9:g.43693721G>A	NCBI36
NG_009832.1:g.29145C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642620.1:c.*268C>T MANE Select	ENSP00000495972.1:n.*268C>T
ENST00000647044.1:c.*268C>T	ENSP00000495811.1:n.*268C>T
ENST00000378062.5:c.*268C>T	ENSP00000367301.5:n.*268C>T
NM_000266.3:c.*268C>T	NP_000257.1:n.*268C>T
NM_000266.4:c.*268C>T MANE Select	NP_000257.1:n.*268C>T