Canonical Allele Identifier: CA1619473592
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32222664_32222666delinsTGG , CM000668.2:g.32222664_32222666delinsTGG GRCh38
NC_000006.11:g.32190441_32190443delinsTGG , CM000668.1:g.32190441_32190443delinsTGG GRCh37
NC_000006.10:g.32298419_32298421delinsTGG NCBI36
NG_028190.1:g.6402_6404delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.296_298delinsCCA MANE Select ENSP00000364163.3:p.Pro99=
ENST00000473562.1:n.425_427delinsCCA
NM_004557.3:c.296_298delinsCCA NP_004548.3:p.Pro99=
NR_134949.1:n.435_437delinsCCA
NR_134950.1:n.435_437delinsCCA
NM_004557.4:c.296_298delinsCCA MANE Select NP_004548.3:p.Pro99=
NR_134949.2:n.435_437delinsCCA
NR_134950.2:n.435_437delinsCCA