Canonical Allele Identifier: CA2324747562
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187003_15187005delinsCAT , CM000681.2:g.15187003_15187005delinsCAT GRCh38
NC_000019.9:g.15297814_15297816delinsCAT , CM000681.1:g.15297814_15297816delinsCAT GRCh37
NC_000019.8:g.15158814_15158816delinsCAT NCBI36
NG_009819.1:g.18977_18979delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1841-17_1841-15delinsATG MANE Select ENSP00000263388.1:n.1841-17_1841-15delinsATG
ENST00000263388.6:c.1841-17_1841-15delinsATG ENSP00000263388.1:n.1841-17_1841-15delinsATG
ENST00000601011.1:c.1838-17_1838-15delinsATG ENSP00000473138.1:n.1838-17_1838-15delinsATG
NM_000435.2:c.1841-17_1841-15delinsATG NP_000426.2:n.1841-17_1841-15delinsATG
XM_005259924.3:c.1841-17_1841-15delinsATG XP_005259981.1:n.1841-17_1841-15delinsATG
XM_005259924.4:c.1841-17_1841-15delinsATG XP_005259981.1:n.1841-17_1841-15delinsATG
NM_000435.3:c.1841-17_1841-15delinsATG MANE Select NP_000426.2:n.1841-17_1841-15delinsATG