Canonical Allele Identifier: CA375644349

Gene: NOTCH1

Linked Data

• ClinVar Variation Id: 1901885
• ClinVar RCV Id: RCV002577309
• dbSNP Id: rs566680728
• MyVariant Identifiers: chr9:g.139399216C>G (hg19) ; chr9:g.136504764C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504764C>G , CM000671.2:g.136504764C>G	GRCh38
NC_000009.11:g.139399216C>G , CM000671.1:g.139399216C>G	GRCh37
NC_000009.10:g.138519037C>G	NCBI36
NG_007458.1:g.46023G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2734G>C
ENST00000651671.1:c.4927G>C MANE Select	ENSP00000498587.1:p.Ala1643Pro
ENST00000679595.1:c.4927G>C	ENSP00000506241.1:p.Ala1643Pro
ENST00000680133.1:c.4813G>C	ENSP00000505319.1:p.Ala1605Pro
ENST00000680218.1:c.4807G>C	ENSP00000505339.1:p.Ala1603Pro
ENST00000680668.1:c.4813G>C	ENSP00000506336.1:p.Ala1605Pro
ENST00000680778.1:c.2524G>C	ENSP00000506033.1:p.Ala842Pro
ENST00000680924.1:c.*2327G>C	ENSP00000506031.1:n.*2327G>C
ENST00000681135.1:c.*2536G>C	ENSP00000506636.1:n.*2536G>C
ENST00000681298.1:n.1740G>C
ENST00000681454.1:c.*4163G>C	ENSP00000505763.1:n.*4163G>C
ENST00000277541.6:c.4927G>C	ENSP00000277541.6:p.Ala1643Pro
ENST00000494783.1:n.82G>C
NM_017617.3:c.4927G>C	NP_060087.3:p.Ala1643Pro
XM_011518717.1:c.4228G>C	XP_011517019.1:p.Ala1410Pro
NM_017617.5:c.4927G>C MANE Select	NP_060087.3:p.Ala1643Pro
XM_011518717.2:c.4204G>C	XP_011517019.2:p.Ala1402Pro