Canonical Allele Identifier: CA1619472829
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220864C= , CM000668.2:g.32220864C= GRCh38
NC_000006.11:g.32188641C= , CM000668.1:g.32188641C= GRCh37
NC_000006.10:g.32296619C= NCBI36
NG_028190.1:g.8204G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.814G= MANE Select ENSP00000364163.3:p.Asp272=
ENST00000473562.1:n.943G=
NM_004557.3:c.814G= NP_004548.3:p.Asp272=
NR_134949.1:n.953G=
NR_134950.1:n.953G=
NM_004557.4:c.814G= MANE Select NP_004548.3:p.Asp272=
NR_134949.2:n.953G=
NR_134950.2:n.953G=