Canonical Allele Identifier: CA2324750065
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192235G= , CM000681.2:g.15192235G= GRCh38
NC_000019.9:g.15303046G= , CM000681.1:g.15303046G= GRCh37
NC_000019.8:g.15164046G= NCBI36
NG_009819.1:g.13747C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.404C= MANE Select ENSP00000263388.1:p.Ser135=
ENST00000263388.6:c.404C= ENSP00000263388.1:p.Ser135=
ENST00000601011.1:c.401C= ENSP00000473138.1:p.Ser134=
NM_000435.2:c.404C= NP_000426.2:p.Ser135=
XM_005259924.3:c.404C= XP_005259981.1:p.Ser135=
XM_005259924.4:c.404C= XP_005259981.1:p.Ser135=
NM_000435.3:c.404C= MANE Select NP_000426.2:p.Ser135=