Canonical Allele Identifier: CA375562930
Gene: NOTCH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136517787T>G , CM000671.2:g.136517787T>G GRCh38
NC_000009.11:g.139412239T>G , CM000671.1:g.139412239T>G GRCh37
NC_000009.10:g.138532060T>G NCBI36
NG_007458.1:g.33000A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651671.1:c.1406A>C MANE Select ENSP00000498587.1:p.Asp469Ala
ENST00000679595.1:c.1406A>C ENSP00000506241.1:p.Asp469Ala
ENST00000680133.1:c.1406A>C ENSP00000505319.1:p.Asp469Ala
ENST00000680218.1:c.1406A>C ENSP00000505339.1:p.Asp469Ala
ENST00000680668.1:c.1406A>C ENSP00000506336.1:p.Asp469Ala
ENST00000680924.1:c.1406A>C ENSP00000506031.1:p.Asp469Ala
ENST00000681135.1:c.1406A>C ENSP00000506636.1:p.Asp469Ala
ENST00000681454.1:c.*642A>C ENSP00000505763.1:n.*642A>C
ENST00000277541.6:c.1406A>C ENSP00000277541.6:p.Asp469Ala
NM_017617.3:c.1406A>C NP_060087.3:p.Asp469Ala
XM_011518717.1:c.707A>C XP_011517019.1:p.Asp236Ala
NM_017617.5:c.1406A>C MANE Select NP_060087.3:p.Asp469Ala
XM_011518717.2:c.683A>C XP_011517019.2:p.Asp228Ala