Canonical Allele Identifier: CA2583064818
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187482_15187483insCCCCCCCCC , CM000681.2:g.15187482_15187483insCCCCCCCCC GRCh38
NC_000019.9:g.15298293_15298294insCCCCCCCCC , CM000681.1:g.15298293_15298294insCCCCCCCCC GRCh37
NC_000019.8:g.15159293_15159294insCCCCCCCCC NCBI36
NG_009819.1:g.18505_18506insGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-139_1607-138insGGGGGGGGG MANE Select ENSP00000263388.1:n.1607-139_1607-138insGGGGGGGGG
ENST00000263388.6:c.1607-139_1607-138insGGGGGGGGG ENSP00000263388.1:n.1607-139_1607-138insGGGGGGGGG
ENST00000601011.1:c.1604-139_1604-138insGGGGGGGGG ENSP00000473138.1:n.1604-139_1604-138insGGGGGGGGG
NM_000435.2:c.1607-139_1607-138insGGGGGGGGG NP_000426.2:n.1607-139_1607-138insGGGGGGGGG
XM_005259924.3:c.1607-139_1607-138insGGGGGGGGG XP_005259981.1:n.1607-139_1607-138insGGGGGGGGG
XM_005259924.4:c.1607-139_1607-138insGGGGGGGGG XP_005259981.1:n.1607-139_1607-138insGGGGGGGGG
NM_000435.3:c.1607-139_1607-138insGGGGGGGGG MANE Select NP_000426.2:n.1607-139_1607-138insGGGGGGGGG