Canonical Allele Identifier: CA404534217
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1356781250

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.404C>T MANE Select ENSP00000263388.1:p.Ser135Leu
ENST00000263388.6:c.404C>T ENSP00000263388.1:p.Ser135Leu
ENST00000601011.1:c.401C>T ENSP00000473138.1:p.Ser134Leu
NM_000435.2:c.404C>T NP_000426.2:p.Ser135Leu
XM_005259924.3:c.404C>T XP_005259981.1:p.Ser135Leu
XM_005259924.4:c.404C>T XP_005259981.1:p.Ser135Leu
NM_000435.3:c.404C>T MANE Select NP_000426.2:p.Ser135Leu