Canonical Allele Identifier: CA163412
Gene: NOTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 139666
ClinVar RCV Id: RCV000128631
dbSNP Id: rs515726231

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136502376del , CM000671.2:g.136502376del GRCh38
NC_000009.11:g.139396828del , CM000671.1:g.139396828del GRCh37
NC_000009.10:g.138516649del NCBI36
NG_007458.1:g.48412del

Transcript Alleles

HGVS Amino-acid change
ENST00000651671.1:c.5281del MANE Select ENSP00000498587.1:p.Arg1761GlyfsTer?
ENST00000679595.1:c.*321del ENSP00000506241.1:n.*321del
ENST00000679969.1:n.470del
ENST00000680003.1:n.321del
ENST00000680133.1:c.5167del ENSP00000505319.1:p.Arg1723GlyfsTer?
ENST00000680218.1:c.5161del ENSP00000505339.1:p.Arg1721GlyfsTer?
ENST00000680668.1:c.5167del ENSP00000506336.1:p.Arg1723GlyfsTer?
ENST00000680778.1:c.2878del ENSP00000506033.1:p.Arg960GlyfsTer?
ENST00000680924.1:c.*2681del ENSP00000506031.1:n.*2681del
ENST00000681135.1:c.*2890del ENSP00000506636.1:n.*2890del
ENST00000681298.1:n.2094del
ENST00000681454.1:c.*4517del ENSP00000505763.1:n.*4517del
ENST00000277541.6:c.5281del ENSP00000277541.6:p.Arg1761GlyfsTer?
NM_017617.3:c.5281del NP_060087.3:p.Arg1761GlyfsTer?
XM_011518717.1:c.4582del XP_011517019.1:p.Arg1528GlyfsTer?
NM_017617.5:c.5281del MANE Select NP_060087.3:p.Arg1761GlyfsTer?
XM_011518717.2:c.4558del XP_011517019.2:p.Arg1520GlyfsTer?