Canonical Allele Identifier: CA1619472713
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1789695392

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220596_32220597dup , CM000668.2:g.32220596_32220597dup GRCh38
NC_000006.11:g.32188373_32188374dup , CM000668.1:g.32188373_32188374dup GRCh37
NC_000006.10:g.32296351_32296352dup NCBI36
NG_028190.1:g.8474_8475dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.970_971dup MANE Select ENSP00000364163.3:p.His325LeufsTer21
ENST00000473562.1:n.1099_1100dup
NM_004557.3:c.970_971dup NP_004548.3:p.His325LeufsTer21
NR_134949.1:n.1109_1110dup
NR_134950.1:n.1109_1110dup
NM_004557.4:c.970_971dup MANE Select NP_004548.3:p.His325LeufsTer21
NR_134949.2:n.1109_1110dup
NR_134950.2:n.1109_1110dup