Canonical Allele Identifier: CA1619472849
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220897A= , CM000668.2:g.32220897A= GRCh38
NC_000006.11:g.32188674A= , CM000668.1:g.32188674A= GRCh37
NC_000006.10:g.32296652A= NCBI36
NG_028190.1:g.8171T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.800-19T= MANE Select ENSP00000364163.3:n.800-19T=
ENST00000473562.1:n.929-19T=
NM_004557.3:c.800-19T= NP_004548.3:n.800-19T=
NR_134949.1:n.939-19T=
NR_134950.1:n.939-19T=
NM_004557.4:c.800-19T= MANE Select NP_004548.3:n.800-19T=
NR_134949.2:n.939-19T=
NR_134950.2:n.939-19T=