Canonical Allele Identifier: CA2564614810
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187471_15187472insGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000681.2:g.15187471_15187472insGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000019.9:g.15298282_15298283insGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000681.1:g.15298282_15298283insGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000019.8:g.15159282_15159283insGGGGGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_009819.1:g.18512_18513insCCCCCCCCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC MANE Select ENSP00000263388.1:n.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCC...
ENST00000263388.6:c.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000263388.1:n.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCC...
ENST00000601011.1:c.1604-132_1604-131insCCCCCCCCCCCCCCCCCCCCCCCCCC ENSP00000473138.1:n.1604-132_1604-131insCCCCCCCCCCCCCCCCCCCCC...
NM_000435.2:c.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC NP_000426.2:n.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC
XM_005259924.3:c.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC XP_005259981.1:n.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCC...
XM_005259924.4:c.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC XP_005259981.1:n.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCC...
NM_000435.3:c.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC MANE Select NP_000426.2:n.1607-132_1607-131insCCCCCCCCCCCCCCCCCCCCCCCCCC