Canonical Allele Identifier: CA375631434

Gene: NOTCH1

Linked Data

• ClinVar Variation Id: 3201355
• ClinVar RCV Id: RCV004488222
• dbSNP Id: rs2133318186
• gnomAD v4: 9-136497221-G-T
• MyVariant Identifiers: chr9:g.139391673G>T (hg19) ; chr9:g.136497221G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497221G>T , CM000671.2:g.136497221G>T	GRCh38
NC_000009.11:g.139391673G>T , CM000671.1:g.139391673G>T	GRCh37
NC_000009.10:g.138511494G>T	NCBI36
NG_007458.1:g.53566C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6518C>A MANE Select	ENSP00000498587.1:p.Ala2173Asp
ENST00000679595.1:c.*1558C>A	ENSP00000506241.1:n.*1558C>A
ENST00000679969.1:n.3114C>A
ENST00000680003.1:n.2850C>A
ENST00000680133.1:c.6404C>A	ENSP00000505319.1:p.Ala2135Asp
ENST00000680218.1:c.6398C>A	ENSP00000505339.1:p.Ala2133Asp
ENST00000680668.1:c.6404C>A	ENSP00000506336.1:p.Ala2135Asp
ENST00000680778.1:c.4115C>A	ENSP00000506033.1:p.Ala1372Asp
ENST00000680924.1:c.*3918C>A	ENSP00000506031.1:n.*3918C>A
ENST00000681135.1:c.*4127C>A	ENSP00000506636.1:n.*4127C>A
ENST00000681298.1:n.4623C>A
ENST00000681454.1:c.*5754C>A	ENSP00000505763.1:n.*5754C>A
ENST00000277541.6:c.6518C>A	ENSP00000277541.6:p.Ala2173Asp
NM_017617.3:c.6518C>A	NP_060087.3:p.Ala2173Asp
XM_011518717.1:c.5819C>A	XP_011517019.1:p.Ala1940Asp
NM_017617.5:c.6518C>A MANE Select	NP_060087.3:p.Ala2173Asp
XM_011518717.2:c.5795C>A	XP_011517019.2:p.Ala1932Asp