Canonical Allele Identifier: CA375644581

Gene: NOTCH1

Linked Data

• gnomAD v4: 9-136504818-C-A
• COSMIC: COSM5647207 ; COSM5647208
• MyVariant Identifiers: chr9:g.139399270C>A (hg19) ; chr9:g.136504818C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504818C>A , CM000671.2:g.136504818C>A	GRCh38
NC_000009.11:g.139399270C>A , CM000671.1:g.139399270C>A	GRCh37
NC_000009.10:g.138519091C>A	NCBI36
NG_007458.1:g.45969G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2680G>T
ENST00000651671.1:c.4873G>T MANE Select	ENSP00000498587.1:p.Glu1625Ter
ENST00000679595.1:c.4873G>T	ENSP00000506241.1:p.Glu1625Ter
ENST00000680133.1:c.4759G>T	ENSP00000505319.1:p.Glu1587Ter
ENST00000680218.1:c.4753G>T	ENSP00000505339.1:p.Glu1585Ter
ENST00000680668.1:c.4759G>T	ENSP00000506336.1:p.Glu1587Ter
ENST00000680778.1:c.2470G>T	ENSP00000506033.1:p.Glu824Ter
ENST00000680924.1:c.*2273G>T	ENSP00000506031.1:n.*2273G>T
ENST00000681135.1:c.*2482G>T	ENSP00000506636.1:n.*2482G>T
ENST00000681298.1:n.1686G>T
ENST00000681454.1:c.*4109G>T	ENSP00000505763.1:n.*4109G>T
ENST00000277541.6:c.4873G>T	ENSP00000277541.6:p.Glu1625Ter
ENST00000494783.1:n.28G>T
NM_017617.3:c.4873G>T	NP_060087.3:p.Glu1625Ter
XM_011518717.1:c.4174G>T	XP_011517019.1:p.Glu1392Ter
NM_017617.5:c.4873G>T MANE Select	NP_060087.3:p.Glu1625Ter
XM_011518717.2:c.4150G>T	XP_011517019.2:p.Glu1384Ter