Canonical Allele Identifier: CA917713570
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1554147270

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202689del , CM000668.2:g.32202689del GRCh38
NC_000006.11:g.32170466del , CM000668.1:g.32170466del GRCh37
NC_000006.10:g.32278444del NCBI36
NG_028190.1:g.26379del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-90del MANE Select ENSP00000364163.3:n.3232-90del
ENST00000474612.1:n.1228del
NM_004557.3:c.3232-90del NP_004548.3:n.3232-90del
NR_134949.1:n.3472+1081del
NR_134950.1:n.3370+1081del
NM_004557.4:c.3232-90del MANE Select NP_004548.3:n.3232-90del
NR_134949.2:n.3472+1081del
NR_134950.2:n.3370+1081del