Canonical Allele Identifier: CA2692643047
Gene: NOTCH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136517947del , CM000671.2:g.136517947del GRCh38
NC_000009.11:g.139412399del , CM000671.1:g.139412399del GRCh37
NC_000009.10:g.138532220del NCBI36
NG_007458.1:g.32842del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651671.1:c.1256-8del MANE Select ENSP00000498587.1:n.1256-8del
ENST00000679595.1:c.1256-8del ENSP00000506241.1:n.1256-8del
ENST00000680133.1:c.1256-8del ENSP00000505319.1:n.1256-8del
ENST00000680218.1:c.1256-8del ENSP00000505339.1:n.1256-8del
ENST00000680668.1:c.1256-8del ENSP00000506336.1:n.1256-8del
ENST00000680924.1:c.1256-8del ENSP00000506031.1:n.1256-8del
ENST00000681135.1:c.1256-8del ENSP00000506636.1:n.1256-8del
ENST00000681454.1:c.*492-8del ENSP00000505763.1:n.*492-8del
ENST00000277541.6:c.1256-8del ENSP00000277541.6:n.1256-8del
NM_017617.3:c.1256-8del NP_060087.3:n.1256-8del
XM_011518717.1:c.557-8del XP_011517019.1:n.557-8del
NM_017617.5:c.1256-8del MANE Select NP_060087.3:n.1256-8del
XM_011518717.2:c.533-8del XP_011517019.2:n.533-8del