Canonical Allele Identifier: CA1087509675
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1788429911

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202655_32202656insT , CM000668.2:g.32202655_32202656insT GRCh38
NC_000006.11:g.32170432_32170433insT , CM000668.1:g.32170432_32170433insT GRCh37
NC_000006.10:g.32278410_32278411insT NCBI36
NG_028190.1:g.26412_26413insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-57_3232-56insA MANE Select ENSP00000364163.3:n.3232-57_3232-56insA
ENST00000474612.1:n.1261_1262insA
NM_004557.3:c.3232-57_3232-56insA NP_004548.3:n.3232-57_3232-56insA
NR_134949.1:n.3472+1114_3472+1115insA
NR_134950.1:n.3370+1114_3370+1115insA
NM_004557.4:c.3232-57_3232-56insA MANE Select NP_004548.3:n.3232-57_3232-56insA
NR_134949.2:n.3472+1114_3472+1115insA
NR_134950.2:n.3370+1114_3370+1115insA