Canonical Allele Identifier: CA2583065562
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191695_15191696insTTGGTAGAGATAGGGTTTTGCC , CM000681.2:g.15191695_15191696insTTGGTAGAGATAGGGTTTTGCC GRCh38
NC_000019.9:g.15302506_15302507insTTGGTAGAGATAGGGTTTTGCC , CM000681.1:g.15302506_15302507insTTGGTAGAGATAGGGTTTTGCC GRCh37
NC_000019.8:g.15163506_15163507insTTGGTAGAGATAGGGTTTTGCC NCBI36
NG_009819.1:g.14287_14288insGCAAAACCCTATCTCTACCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.803-38_803-37insGCAAAACCCTATCTCTACCAAG MANE Select ENSP00000263388.1:n.803-38_803-37insGCAAAACCCTATCTCTACCAAG
ENST00000263388.6:c.803-38_803-37insGCAAAACCCTATCTCTACCAAG ENSP00000263388.1:n.803-38_803-37insGCAAAACCCTATCTCTACCAAG
ENST00000601011.1:c.800-38_800-37insGCAAAACCCTATCTCTACCAAG ENSP00000473138.1:n.800-38_800-37insGCAAAACCCTATCTCTACCAAG
NM_000435.2:c.803-38_803-37insGCAAAACCCTATCTCTACCAAG NP_000426.2:n.803-38_803-37insGCAAAACCCTATCTCTACCAAG
XM_005259924.3:c.803-38_803-37insGCAAAACCCTATCTCTACCAAG XP_005259981.1:n.803-38_803-37insGCAAAACCCTATCTCTACCAAG
XM_005259924.4:c.803-38_803-37insGCAAAACCCTATCTCTACCAAG XP_005259981.1:n.803-38_803-37insGCAAAACCCTATCTCTACCAAG
NM_000435.3:c.803-38_803-37insGCAAAACCCTATCTCTACCAAG MANE Select NP_000426.2:n.803-38_803-37insGCAAAACCCTATCTCTACCAAG