Canonical Allele Identifier: CA2324744288
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180217C= , CM000681.2:g.15180217C= GRCh38
NC_000019.9:g.15291028C= , CM000681.1:g.15291028C= GRCh37
NC_000019.8:g.15152028C= NCBI36
NG_009819.1:g.25765G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.3182G= MANE Select ENSP00000263388.1:p.Cys1061=
ENST00000263388.6:c.3182G= ENSP00000263388.1:p.Cys1061=
ENST00000601011.1:c.3023G= ENSP00000473138.1:p.Cys1008=
NM_000435.2:c.3182G= NP_000426.2:p.Cys1061=
XM_005259924.3:c.3026G= XP_005259981.1:p.Cys1009=
XM_005259924.4:c.3026G= XP_005259981.1:p.Cys1009=
NM_000435.3:c.3182G= MANE Select NP_000426.2:p.Cys1061=