Canonical Allele Identifier: CA2711382909
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs2127487182

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220454_32220499del , CM000668.2:g.32220454_32220499del GRCh38
NC_000006.11:g.32188231_32188276del , CM000668.1:g.32188231_32188276del GRCh37
NC_000006.10:g.32296209_32296254del NCBI36
NG_028190.1:g.8569_8614del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.1065_1110del MANE Select ENSP00000364163.3:p.Asn355LysfsTer28
ENST00000473562.1:n.1194_1239del
NM_004557.3:c.1065_1110del NP_004548.3:p.Asn355LysfsTer28
NR_134949.1:n.1204_1249del
NR_134950.1:n.1204_1249del
NM_004557.4:c.1065_1110del MANE Select NP_004548.3:p.Asn355LysfsTer28
NR_134949.2:n.1204_1249del
NR_134950.2:n.1204_1249del