Canonical Allele Identifier: CA375644278

Gene: NOTCH1

Linked Data

• COSMIC: COSM33751 ; COSM5678633
• MyVariant Identifiers: chr9:g.139399195C>T (hg19) ; chr9:g.136504743C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504743C>T , CM000671.2:g.136504743C>T	GRCh38
NC_000009.11:g.139399195C>T , CM000671.1:g.139399195C>T	GRCh37
NC_000009.10:g.138519016C>T	NCBI36
NG_007458.1:g.46044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2755G>A
ENST00000651671.1:c.4948G>A MANE Select	ENSP00000498587.1:p.Ala1650Thr
ENST00000679595.1:c.4948G>A	ENSP00000506241.1:p.Ala1650Thr
ENST00000680133.1:c.4834G>A	ENSP00000505319.1:p.Ala1612Thr
ENST00000680218.1:c.4828G>A	ENSP00000505339.1:p.Ala1610Thr
ENST00000680668.1:c.4834G>A	ENSP00000506336.1:p.Ala1612Thr
ENST00000680778.1:c.2545G>A	ENSP00000506033.1:p.Ala849Thr
ENST00000680924.1:c.*2348G>A	ENSP00000506031.1:n.*2348G>A
ENST00000681135.1:c.*2557G>A	ENSP00000506636.1:n.*2557G>A
ENST00000681298.1:n.1761G>A
ENST00000681454.1:c.*4184G>A	ENSP00000505763.1:n.*4184G>A
ENST00000277541.6:c.4948G>A	ENSP00000277541.6:p.Ala1650Thr
ENST00000494783.1:n.103G>A
NM_017617.3:c.4948G>A	NP_060087.3:p.Ala1650Thr
XM_011518717.1:c.4249G>A	XP_011517019.1:p.Ala1417Thr
NM_017617.5:c.4948G>A MANE Select	NP_060087.3:p.Ala1650Thr
XM_011518717.2:c.4225G>A	XP_011517019.2:p.Ala1409Thr