Canonical Allele Identifier: CA375644036

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1843049242
• MyVariant Identifiers: chr9:g.139399143T>A (hg19) ; chr9:g.136504691T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504691T>A , CM000671.2:g.136504691T>A	GRCh38
NC_000009.11:g.139399143T>A , CM000671.1:g.139399143T>A	GRCh37
NC_000009.10:g.138518964T>A	NCBI36
NG_007458.1:g.46096A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2807A>T
ENST00000651671.1:c.5000A>T MANE Select	ENSP00000498587.1:p.Asp1667Val
ENST00000679595.1:c.5000A>T	ENSP00000506241.1:p.Asp1667Val
ENST00000680133.1:c.4886A>T	ENSP00000505319.1:p.Asp1629Val
ENST00000680218.1:c.4880A>T	ENSP00000505339.1:p.Asp1627Val
ENST00000680668.1:c.4886A>T	ENSP00000506336.1:p.Asp1629Val
ENST00000680778.1:c.2597A>T	ENSP00000506033.1:p.Asp866Val
ENST00000680924.1:c.*2400A>T	ENSP00000506031.1:n.*2400A>T
ENST00000681135.1:c.*2609A>T	ENSP00000506636.1:n.*2609A>T
ENST00000681298.1:n.1813A>T
ENST00000681454.1:c.*4236A>T	ENSP00000505763.1:n.*4236A>T
ENST00000277541.6:c.5000A>T	ENSP00000277541.6:p.Asp1667Val
ENST00000494783.1:n.155A>T
NM_017617.3:c.5000A>T	NP_060087.3:p.Asp1667Val
XM_011518717.1:c.4301A>T	XP_011517019.1:p.Asp1434Val
NM_017617.5:c.5000A>T MANE Select	NP_060087.3:p.Asp1667Val
XM_011518717.2:c.4277A>T	XP_011517019.2:p.Asp1426Val