Canonical Allele Identifier: CA2695233467

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949803del , CM000685.2:g.43949803del GRCh38
NC_000023.10:g.43809049del , CM000685.1:g.43809049del GRCh37
NC_000023.9:g.43693993del NCBI36
NG_009832.1:g.28874del

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.399del (NDP) MANE Select ENSP00000495972.1:p.Ter134GluextTer?
ENST00000647044.1:c.399del (NDP) ENSP00000495811.1:p.Ter134GluextTer?
ENST00000378062.5:c.399del (NDP) ENSP00000367301.5:p.Ter134GluextTer?
ENST00000470584.1:n.443del (NDP)
NM_000266.3:c.399del (NDP) NP_000257.1:p.Ter134GluextTer?
NR_046631.1:n.72del (NDP-AS1)
NM_000266.4:c.399del (NDP) MANE Select NP_000257.1:p.Ter134GluextTer?