Canonical Allele Identifier: CA1619472689
Gene: NOTCH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220534C= , CM000668.2:g.32220534C= GRCh38
NC_000006.11:g.32188311C= , CM000668.1:g.32188311C= GRCh37
NC_000006.10:g.32296289C= NCBI36
NG_028190.1:g.8534G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.1030G= MANE Select ENSP00000364163.3:p.Val344=
ENST00000473562.1:n.1159G=
NM_004557.3:c.1030G= NP_004548.3:p.Val344=
NR_134949.1:n.1169G=
NR_134950.1:n.1169G=
NM_004557.4:c.1030G= MANE Select NP_004548.3:p.Val344=
NR_134949.2:n.1169G=
NR_134950.2:n.1169G=
Search 100 bp 5'
Search 100 bp 3'