Canonical Allele Identifier: CA1619472824
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220847T= , CM000668.2:g.32220847T= GRCh38
NC_000006.11:g.32188624T= , CM000668.1:g.32188624T= GRCh37
NC_000006.10:g.32296602T= NCBI36
NG_028190.1:g.8221A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.831A= MANE Select ENSP00000364163.3:p.Pro277=
ENST00000473562.1:n.960A=
NM_004557.3:c.831A= NP_004548.3:p.Pro277=
NR_134949.1:n.970A=
NR_134950.1:n.970A=
NM_004557.4:c.831A= MANE Select NP_004548.3:p.Pro277=
NR_134949.2:n.970A=
NR_134950.2:n.970A=