Canonical Allele Identifier: CA645543460

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133336888
• COSMIC: COSM13051

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504915_136504916insGCT , CM000671.2:g.136504915_136504916insGCT	GRCh38
NC_000009.11:g.139399367_139399368insGCT , CM000671.1:g.139399367_139399368insGCT	GRCh37
NC_000009.10:g.138519188_138519189insGCT	NCBI36
NG_007458.1:g.45871_45872insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2582_2583insAGC
ENST00000651671.1:c.4775_4776insAGC MANE Select	ENSP00000498587.1:p.Phe1592delinsLeuAla
ENST00000679595.1:c.4775_4776insAGC	ENSP00000506241.1:p.Phe1592delinsLeuAla
ENST00000680133.1:c.4661_4662insAGC	ENSP00000505319.1:p.Phe1554delinsLeuAla
ENST00000680218.1:c.4655_4656insAGC	ENSP00000505339.1:p.Phe1552delinsLeuAla
ENST00000680668.1:c.4661_4662insAGC	ENSP00000506336.1:p.Phe1554delinsLeuAla
ENST00000680778.1:c.2372_2373insAGC	ENSP00000506033.1:p.Phe791delinsLeuAla
ENST00000680924.1:c.*2175_*2176insAGC	ENSP00000506031.1:n.*2175_*2176insAGC
ENST00000681135.1:c.*2384_*2385insAGC	ENSP00000506636.1:n.*2384_*2385insAGC
ENST00000681298.1:n.1588_1589insAGC
ENST00000681454.1:c.*4011_*4012insAGC	ENSP00000505763.1:n.*4011_*4012insAGC
ENST00000277541.6:c.4775_4776insAGC	ENSP00000277541.6:p.Phe1592delinsLeuAla
NM_017617.3:c.4775_4776insAGC	NP_060087.3:p.Phe1592delinsLeuAla
XM_011518717.1:c.4076_4077insAGC	XP_011517019.1:p.Phe1359delinsLeuAla
NM_017617.5:c.4775_4776insAGC MANE Select	NP_060087.3:p.Phe1592delinsLeuAla
XM_011518717.2:c.4052_4053insAGC	XP_011517019.2:p.Phe1351delinsLeuAla