Canonical Allele Identifier: CA375631412

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133318164
• MyVariant Identifiers: chr9:g.139391668C>T (hg19) ; chr9:g.136497216C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497216C>T , CM000671.2:g.136497216C>T	GRCh38
NC_000009.11:g.139391668C>T , CM000671.1:g.139391668C>T	GRCh37
NC_000009.10:g.138511489C>T	NCBI36
NG_007458.1:g.53571G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6523G>A MANE Select	ENSP00000498587.1:p.Asp2175Asn
ENST00000679595.1:c.*1563G>A	ENSP00000506241.1:n.*1563G>A
ENST00000679969.1:n.3119G>A
ENST00000680003.1:n.2855G>A
ENST00000680133.1:c.6409G>A	ENSP00000505319.1:p.Asp2137Asn
ENST00000680218.1:c.6403G>A	ENSP00000505339.1:p.Asp2135Asn
ENST00000680668.1:c.6409G>A	ENSP00000506336.1:p.Asp2137Asn
ENST00000680778.1:c.4120G>A	ENSP00000506033.1:p.Asp1374Asn
ENST00000680924.1:c.*3923G>A	ENSP00000506031.1:n.*3923G>A
ENST00000681135.1:c.*4132G>A	ENSP00000506636.1:n.*4132G>A
ENST00000681298.1:n.4628G>A
ENST00000681454.1:c.*5759G>A	ENSP00000505763.1:n.*5759G>A
ENST00000277541.6:c.6523G>A	ENSP00000277541.6:p.Asp2175Asn
NM_017617.3:c.6523G>A	NP_060087.3:p.Asp2175Asn
XM_011518717.1:c.5824G>A	XP_011517019.1:p.Asp1942Asn
NM_017617.5:c.6523G>A MANE Select	NP_060087.3:p.Asp2175Asn
XM_011518717.2:c.5800G>A	XP_011517019.2:p.Asp1934Asn