Canonical Allele Identifier: CA2693514195

Gene: NDP

Linked Data

• gnomAD v4: X-43949709-TGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43949710_43949712del , CM000685.2:g.43949710_43949712del	GRCh38
NC_000023.10:g.43808956_43808958del , CM000685.1:g.43808956_43808958del	GRCh37
NC_000023.9:g.43693900_43693902del	NCBI36
NG_009832.1:g.28964_28966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642620.1:c.*87_*89del MANE Select	ENSP00000495972.1:n.*87_*89del
ENST00000647044.1:c.*87_*89del	ENSP00000495811.1:n.*87_*89del
ENST00000378062.5:c.*87_*89del	ENSP00000367301.5:n.*87_*89del
ENST00000470584.1:n.533_535del
NM_000266.3:c.*87_*89del	NP_000257.1:n.*87_*89del
NM_000266.4:c.*87_*89del MANE Select	NP_000257.1:n.*87_*89del