Canonical Allele Identifier: CA2324747744
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2046891456

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187350del , CM000681.2:g.15187350del GRCh38
NC_000019.9:g.15298161del , CM000681.1:g.15298161del GRCh37
NC_000019.8:g.15159161del NCBI36
NG_009819.1:g.18633del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-11del MANE Select ENSP00000263388.1:n.1607-11del
ENST00000263388.6:c.1607-11del ENSP00000263388.1:n.1607-11del
ENST00000601011.1:c.1604-11del ENSP00000473138.1:n.1604-11del
NM_000435.2:c.1607-11del NP_000426.2:n.1607-11del
XM_005259924.3:c.1607-11del XP_005259981.1:n.1607-11del
XM_005259924.4:c.1607-11del XP_005259981.1:n.1607-11del
NM_000435.3:c.1607-11del MANE Select NP_000426.2:n.1607-11del