Canonical Allele Identifier: CA2324750062
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192225G= , CM000681.2:g.15192225G= GRCh38
NC_000019.9:g.15303036G= , CM000681.1:g.15303036G= GRCh37
NC_000019.8:g.15164036G= NCBI36
NG_009819.1:g.13757C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.414C= MANE Select ENSP00000263388.1:p.Pro138=
ENST00000263388.6:c.414C= ENSP00000263388.1:p.Pro138=
ENST00000601011.1:c.411C= ENSP00000473138.1:p.Pro137=
NM_000435.2:c.414C= NP_000426.2:p.Pro138=
XM_005259924.3:c.414C= XP_005259981.1:p.Pro138=
XM_005259924.4:c.414C= XP_005259981.1:p.Pro138=
NM_000435.3:c.414C= MANE Select NP_000426.2:p.Pro138=