Canonical Allele Identifier: CA1619467800
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1788442579

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202902_32202906del , CM000668.2:g.32202902_32202906del GRCh38
NC_000006.11:g.32170679_32170683del , CM000668.1:g.32170679_32170683del GRCh37
NC_000006.10:g.32278657_32278661del NCBI36
NG_028190.1:g.26168_26172del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-301_3232-297del MANE Select ENSP00000364163.3:n.3232-301_3232-297del
ENST00000474612.1:n.1017_1021del
NM_004557.3:c.3232-301_3232-297del NP_004548.3:n.3232-301_3232-297del
NR_134949.1:n.3472+870_3472+874del
NR_134950.1:n.3370+870_3370+874del
NM_004557.4:c.3232-301_3232-297del MANE Select NP_004548.3:n.3232-301_3232-297del
NR_134949.2:n.3472+870_3472+874del
NR_134950.2:n.3370+870_3370+874del