Canonical Allele Identifier: CA2583064858

Gene: NOTCH3

Linked Data

• gnomAD v4: 19-15187480-C-CCCCCCCCCCCCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15187482_15187483insCCCCCCCCCCCACC , CM000681.2:g.15187482_15187483insCCCCCCCCCCCACC	GRCh38
NC_000019.9:g.15298293_15298294insCCCCCCCCCCCACC , CM000681.1:g.15298293_15298294insCCCCCCCCCCCACC	GRCh37
NC_000019.8:g.15159293_15159294insCCCCCCCCCCCACC	NCBI36
NG_009819.1:g.18501_18502insTGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.1607-143_1607-142insTGGGGGGGGGGGGG MANE Select	ENSP00000263388.1:n.1607-143_1607-142insTGGGGGGGGGGGGG
ENST00000263388.6:c.1607-143_1607-142insTGGGGGGGGGGGGG	ENSP00000263388.1:n.1607-143_1607-142insTGGGGGGGGGGGGG
ENST00000601011.1:c.1604-143_1604-142insTGGGGGGGGGGGGG	ENSP00000473138.1:n.1604-143_1604-142insTGGGGGGGGGGGGG
NM_000435.2:c.1607-143_1607-142insTGGGGGGGGGGGGG	NP_000426.2:n.1607-143_1607-142insTGGGGGGGGGGGGG
XM_005259924.3:c.1607-143_1607-142insTGGGGGGGGGGGGG	XP_005259981.1:n.1607-143_1607-142insTGGGGGGGGGGGGG
XM_005259924.4:c.1607-143_1607-142insTGGGGGGGGGGGGG	XP_005259981.1:n.1607-143_1607-142insTGGGGGGGGGGGGG
NM_000435.3:c.1607-143_1607-142insTGGGGGGGGGGGGG MANE Select	NP_000426.2:n.1607-143_1607-142insTGGGGGGGGGGGGG