Canonical Allele Identifier: CA1619472752
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220665G= , CM000668.2:g.32220665G= GRCh38
NC_000006.11:g.32188442G= , CM000668.1:g.32188442G= GRCh37
NC_000006.10:g.32296420G= NCBI36
NG_028190.1:g.8403C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.923-24C= MANE Select ENSP00000364163.3:n.923-24C=
ENST00000473562.1:n.1052-24C=
NM_004557.3:c.923-24C= NP_004548.3:n.923-24C=
NR_134949.1:n.1062-24C=
NR_134950.1:n.1062-24C=
NM_004557.4:c.923-24C= MANE Select NP_004548.3:n.923-24C=
NR_134949.2:n.1062-24C=
NR_134950.2:n.1062-24C=