Canonical Allele Identifier: CA2678138109
Gene: NOTCH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220703del , CM000668.2:g.32220703del GRCh38
NC_000006.11:g.32188480del , CM000668.1:g.32188480del GRCh37
NC_000006.10:g.32296458del NCBI36
NG_028190.1:g.8365del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.922+53del MANE Select ENSP00000364163.3:n.922+53del
ENST00000473562.1:n.1051+53del
NM_004557.3:c.922+53del NP_004548.3:n.922+53del
NR_134949.1:n.1061+53del
NR_134950.1:n.1061+53del
NM_004557.4:c.922+53del MANE Select NP_004548.3:n.922+53del
NR_134949.2:n.1061+53del
NR_134950.2:n.1061+53del