Canonical Allele Identifier: CA375564490
Gene: NOTCH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136518167A>T , CM000671.2:g.136518167A>T GRCh38
NC_000009.11:g.139412619A>T , CM000671.1:g.139412619A>T GRCh37
NC_000009.10:g.138532440A>T NCBI36
NG_007458.1:g.32620T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651671.1:c.1225T>A MANE Select ENSP00000498587.1:p.Cys409Ser
ENST00000679595.1:c.1225T>A ENSP00000506241.1:p.Cys409Ser
ENST00000680133.1:c.1225T>A ENSP00000505319.1:p.Cys409Ser
ENST00000680218.1:c.1225T>A ENSP00000505339.1:p.Cys409Ser
ENST00000680668.1:c.1225T>A ENSP00000506336.1:p.Cys409Ser
ENST00000680924.1:c.1225T>A ENSP00000506031.1:p.Cys409Ser
ENST00000681135.1:c.1225T>A ENSP00000506636.1:p.Cys409Ser
ENST00000681454.1:c.*461T>A ENSP00000505763.1:n.*461T>A
ENST00000277541.6:c.1225T>A ENSP00000277541.6:p.Cys409Ser
NM_017617.3:c.1225T>A NP_060087.3:p.Cys409Ser
XM_011518717.1:c.526T>A XP_011517019.1:p.Cys176Ser
NM_017617.5:c.1225T>A MANE Select NP_060087.3:p.Cys409Ser
XM_011518717.2:c.502T>A XP_011517019.2:p.Cys168Ser