Canonical Allele Identifier: CA1619472801
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220783T= , CM000668.2:g.32220783T= GRCh38
NC_000006.11:g.32188560T= , CM000668.1:g.32188560T= GRCh37
NC_000006.10:g.32296538T= NCBI36
NG_028190.1:g.8285A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.895A= MANE Select ENSP00000364163.3:p.Thr299=
ENST00000473562.1:n.1024A=
NM_004557.3:c.895A= NP_004548.3:p.Thr299=
NR_134949.1:n.1034A=
NR_134950.1:n.1034A=
NM_004557.4:c.895A= MANE Select NP_004548.3:p.Thr299=
NR_134949.2:n.1034A=
NR_134950.2:n.1034A=