Canonical Allele Identifier: CA645543421
Gene: NOTCH1 HGNC NCBI

Linked Data

dbSNP Id: rs2133336611
COSMIC: COSM21895

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136504873_136504874insGGGTCC , CM000671.2:g.136504873_136504874insGGGTCC GRCh38
NC_000009.11:g.139399325_139399326insGGGTCC , CM000671.1:g.139399325_139399326insGGGTCC GRCh37
NC_000009.10:g.138519146_138519147insGGGTCC NCBI36
NG_007458.1:g.45913_45914insGGACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645828.1:n.2624_2625insGGACCC
ENST00000651671.1:c.4817_4818insGGACCC MANE Select ENSP00000498587.1:p.Phe1606delinsLeuAspPro
ENST00000679595.1:c.4817_4818insGGACCC ENSP00000506241.1:p.Phe1606delinsLeuAspPro
ENST00000680133.1:c.4703_4704insGGACCC ENSP00000505319.1:p.Phe1568delinsLeuAspPro
ENST00000680218.1:c.4697_4698insGGACCC ENSP00000505339.1:p.Phe1566delinsLeuAspPro
ENST00000680668.1:c.4703_4704insGGACCC ENSP00000506336.1:p.Phe1568delinsLeuAspPro
ENST00000680778.1:c.2414_2415insGGACCC ENSP00000506033.1:p.Phe805delinsLeuAspPro
ENST00000680924.1:c.*2217_*2218insGGACCC ENSP00000506031.1:n.*2217_*2218insGGACCC
ENST00000681135.1:c.*2426_*2427insGGACCC ENSP00000506636.1:n.*2426_*2427insGGACCC
ENST00000681298.1:n.1630_1631insGGACCC
ENST00000681454.1:c.*4053_*4054insGGACCC ENSP00000505763.1:n.*4053_*4054insGGACCC
ENST00000277541.6:c.4817_4818insGGACCC ENSP00000277541.6:p.Phe1606delinsLeuAspPro
NM_017617.3:c.4817_4818insGGACCC NP_060087.3:p.Phe1606delinsLeuAspPro
XM_011518717.1:c.4118_4119insGGACCC XP_011517019.1:p.Phe1373delinsLeuAspPro
NM_017617.5:c.4817_4818insGGACCC MANE Select NP_060087.3:p.Phe1606delinsLeuAspPro
XM_011518717.2:c.4094_4095insGGACCC XP_011517019.2:p.Phe1365delinsLeuAspPro