Canonical Allele Identifier: CA2324744201
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2046826040

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180035del , CM000681.2:g.15180035del GRCh38
NC_000019.9:g.15290846del , CM000681.1:g.15290846del GRCh37
NC_000019.8:g.15151846del NCBI36
NG_009819.1:g.25949del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3327+39del MANE Select ENSP00000263388.1:n.3327+39del
ENST00000263388.6:c.3327+39del ENSP00000263388.1:n.3327+39del
ENST00000601011.1:c.3168+39del ENSP00000473138.1:n.3168+39del
NM_000435.2:c.3327+39del NP_000426.2:n.3327+39del
XM_005259924.3:c.3171+39del XP_005259981.1:n.3171+39del
XM_005259924.4:c.3171+39del XP_005259981.1:n.3171+39del
NM_000435.3:c.3327+39del MANE Select NP_000426.2:n.3327+39del