Canonical Allele Identifier: CA375644430

Gene: NOTCH1

Linked Data

• ClinVar Variation Id: 2632167
• ClinVar RCV Id: RCV004528606
• dbSNP Id: rs764006572
• MyVariant Identifiers: chr9:g.139399237C>A (hg19) ; chr9:g.136504785C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504785C>A , CM000671.2:g.136504785C>A	GRCh38
NC_000009.11:g.139399237C>A , CM000671.1:g.139399237C>A	GRCh37
NC_000009.10:g.138519058C>A	NCBI36
NG_007458.1:g.46002G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2713G>T
ENST00000651671.1:c.4906G>T MANE Select	ENSP00000498587.1:p.Glu1636Ter
ENST00000679595.1:c.4906G>T	ENSP00000506241.1:p.Glu1636Ter
ENST00000680133.1:c.4792G>T	ENSP00000505319.1:p.Glu1598Ter
ENST00000680218.1:c.4786G>T	ENSP00000505339.1:p.Glu1596Ter
ENST00000680668.1:c.4792G>T	ENSP00000506336.1:p.Glu1598Ter
ENST00000680778.1:c.2503G>T	ENSP00000506033.1:p.Glu835Ter
ENST00000680924.1:c.*2306G>T	ENSP00000506031.1:n.*2306G>T
ENST00000681135.1:c.*2515G>T	ENSP00000506636.1:n.*2515G>T
ENST00000681298.1:n.1719G>T
ENST00000681454.1:c.*4142G>T	ENSP00000505763.1:n.*4142G>T
ENST00000277541.6:c.4906G>T	ENSP00000277541.6:p.Glu1636Ter
ENST00000494783.1:n.61G>T
NM_017617.3:c.4906G>T	NP_060087.3:p.Glu1636Ter
XM_011518717.1:c.4207G>T	XP_011517019.1:p.Glu1403Ter
NM_017617.5:c.4906G>T MANE Select	NP_060087.3:p.Glu1636Ter
XM_011518717.2:c.4183G>T	XP_011517019.2:p.Glu1395Ter