Canonical Allele Identifier: CA2324747772
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2046891897

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187388_15187389insTC , CM000681.2:g.15187388_15187389insTC GRCh38
NC_000019.9:g.15298199_15298200insTC , CM000681.1:g.15298199_15298200insTC GRCh37
NC_000019.8:g.15159199_15159200insTC NCBI36
NG_009819.1:g.18593_18594insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-51_1607-50insGA MANE Select ENSP00000263388.1:n.1607-51_1607-50insGA
ENST00000263388.6:c.1607-51_1607-50insGA ENSP00000263388.1:n.1607-51_1607-50insGA
ENST00000601011.1:c.1604-51_1604-50insGA ENSP00000473138.1:n.1604-51_1604-50insGA
NM_000435.2:c.1607-51_1607-50insGA NP_000426.2:n.1607-51_1607-50insGA
XM_005259924.3:c.1607-51_1607-50insGA XP_005259981.1:n.1607-51_1607-50insGA
XM_005259924.4:c.1607-51_1607-50insGA XP_005259981.1:n.1607-51_1607-50insGA
NM_000435.3:c.1607-51_1607-50insGA MANE Select NP_000426.2:n.1607-51_1607-50insGA