Canonical Allele Identifier: CA2324750041
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192198T= , CM000681.2:g.15192198T= GRCh38
NC_000019.9:g.15303009T= , CM000681.1:g.15303009T= GRCh37
NC_000019.8:g.15164009T= NCBI36
NG_009819.1:g.13784A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.441A= MANE Select ENSP00000263388.1:p.Pro147=
ENST00000263388.6:c.441A= ENSP00000263388.1:p.Pro147=
ENST00000601011.1:c.438A= ENSP00000473138.1:p.Pro146=
NM_000435.2:c.441A= NP_000426.2:p.Pro147=
XM_005259924.3:c.441A= XP_005259981.1:p.Pro147=
XM_005259924.4:c.441A= XP_005259981.1:p.Pro147=
NM_000435.3:c.441A= MANE Select NP_000426.2:p.Pro147=