Canonical Allele Identifier: CA2324744240
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180106G= , CM000681.2:g.15180106G= GRCh38
NC_000019.9:g.15290917G= , CM000681.1:g.15290917G= GRCh37
NC_000019.8:g.15151917G= NCBI36
NG_009819.1:g.25876C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3293C= MANE Select ENSP00000263388.1:p.Thr1098=
ENST00000263388.6:c.3293C= ENSP00000263388.1:p.Thr1098=
ENST00000601011.1:c.3134C= ENSP00000473138.1:p.Thr1045=
NM_000435.2:c.3293C= NP_000426.2:p.Thr1098=
XM_005259924.3:c.3137C= XP_005259981.1:p.Thr1046=
XM_005259924.4:c.3137C= XP_005259981.1:p.Thr1046=
NM_000435.3:c.3293C= MANE Select NP_000426.2:p.Thr1098=