Canonical Allele Identifier: CA2581974334
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187471_15187472insGGGG , CM000681.2:g.15187471_15187472insGGGG GRCh38
NC_000019.9:g.15298282_15298283insGGGG , CM000681.1:g.15298282_15298283insGGGG GRCh37
NC_000019.8:g.15159282_15159283insGGGG NCBI36
NG_009819.1:g.18512_18513insCCCC

Transcript Alleles

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