Canonical Allele Identifier: CA375644348

Gene: NOTCH1

Linked Data

• dbSNP Id: rs566680728
• gnomAD v4: 9-136504764-C-A
• MyVariant Identifiers: chr9:g.139399216C>A (hg19) ; chr9:g.136504764C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2734G>T
ENST00000651671.1:c.4927G>T MANE Select	ENSP00000498587.1:p.Ala1643Ser
ENST00000679595.1:c.4927G>T	ENSP00000506241.1:p.Ala1643Ser
ENST00000680133.1:c.4813G>T	ENSP00000505319.1:p.Ala1605Ser
ENST00000680218.1:c.4807G>T	ENSP00000505339.1:p.Ala1603Ser
ENST00000680668.1:c.4813G>T	ENSP00000506336.1:p.Ala1605Ser
ENST00000680778.1:c.2524G>T	ENSP00000506033.1:p.Ala842Ser
ENST00000680924.1:c.*2327G>T	ENSP00000506031.1:n.*2327G>T
ENST00000681135.1:c.*2536G>T	ENSP00000506636.1:n.*2536G>T
ENST00000681298.1:n.1740G>T
ENST00000681454.1:c.*4163G>T	ENSP00000505763.1:n.*4163G>T
ENST00000277541.6:c.4927G>T	ENSP00000277541.6:p.Ala1643Ser
ENST00000494783.1:n.82G>T
NM_017617.3:c.4927G>T	NP_060087.3:p.Ala1643Ser
XM_011518717.1:c.4228G>T	XP_011517019.1:p.Ala1410Ser
NM_017617.5:c.4927G>T MANE Select	NP_060087.3:p.Ala1643Ser
XM_011518717.2:c.4204G>T	XP_011517019.2:p.Ala1402Ser