Canonical Allele Identifier: CA2324749915

Gene: NOTCH3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15191929_15191931delinsCCT , CM000681.2:g.15191929_15191931delinsCCT	GRCh38
NC_000019.9:g.15302740_15302742delinsCCT , CM000681.1:g.15302740_15302742delinsCCT	GRCh37
NC_000019.8:g.15163740_15163742delinsCCT	NCBI36
NG_009819.1:g.14051_14053delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.679+29_679+31delinsAGG MANE Select	ENSP00000263388.1:n.679+29_679+31delinsAGG
ENST00000263388.6:c.679+29_679+31delinsAGG	ENSP00000263388.1:n.679+29_679+31delinsAGG
ENST00000601011.1:c.676+29_676+31delinsAGG	ENSP00000473138.1:n.676+29_676+31delinsAGG
NM_000435.2:c.679+29_679+31delinsAGG	NP_000426.2:n.679+29_679+31delinsAGG
XM_005259924.3:c.679+29_679+31delinsAGG	XP_005259981.1:n.679+29_679+31delinsAGG
XM_005259924.4:c.679+29_679+31delinsAGG	XP_005259981.1:n.679+29_679+31delinsAGG
NM_000435.3:c.679+29_679+31delinsAGG MANE Select	NP_000426.2:n.679+29_679+31delinsAGG