Canonical Allele Identifier: CA1619467725
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202666_32202668delinsACT , CM000668.2:g.32202666_32202668delinsACT GRCh38
NC_000006.11:g.32170443_32170445delinsACT , CM000668.1:g.32170443_32170445delinsACT GRCh37
NC_000006.10:g.32278421_32278423delinsACT NCBI36
NG_028190.1:g.26400_26402delinsAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-69_3232-67delinsAGT MANE Select ENSP00000364163.3:n.3232-69_3232-67delinsAGT
ENST00000474612.1:n.1249_1251delinsAGT
NM_004557.3:c.3232-69_3232-67delinsAGT NP_004548.3:n.3232-69_3232-67delinsAGT
NR_134949.1:n.3472+1102_3472+1104delinsAGT
NR_134950.1:n.3370+1102_3370+1104delinsAGT
NM_004557.4:c.3232-69_3232-67delinsAGT MANE Select NP_004548.3:n.3232-69_3232-67delinsAGT
NR_134949.2:n.3472+1102_3472+1104delinsAGT
NR_134950.2:n.3370+1102_3370+1104delinsAGT