Canonical Allele Identifier: CA375645127

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1843055486
• gnomAD v4: 9-136504928-C-A
• MyVariant Identifiers: chr9:g.139399380C>A (hg19) ; chr9:g.136504928C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504928C>A , CM000671.2:g.136504928C>A	GRCh38
NC_000009.11:g.139399380C>A , CM000671.1:g.139399380C>A	GRCh37
NC_000009.10:g.138519201C>A	NCBI36
NG_007458.1:g.45859G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2570G>T
ENST00000651671.1:c.4763G>T MANE Select	ENSP00000498587.1:p.Ser1588Ile
ENST00000679595.1:c.4763G>T	ENSP00000506241.1:p.Ser1588Ile
ENST00000680133.1:c.4649G>T	ENSP00000505319.1:p.Ser1550Ile
ENST00000680218.1:c.4643G>T	ENSP00000505339.1:p.Ser1548Ile
ENST00000680668.1:c.4649G>T	ENSP00000506336.1:p.Ser1550Ile
ENST00000680778.1:c.2360G>T	ENSP00000506033.1:p.Ser787Ile
ENST00000680924.1:c.*2163G>T	ENSP00000506031.1:n.*2163G>T
ENST00000681135.1:c.*2372G>T	ENSP00000506636.1:n.*2372G>T
ENST00000681298.1:n.1576G>T
ENST00000681454.1:c.*3999G>T	ENSP00000505763.1:n.*3999G>T
ENST00000277541.6:c.4763G>T	ENSP00000277541.6:p.Ser1588Ile
NM_017617.3:c.4763G>T	NP_060087.3:p.Ser1588Ile
XM_011518717.1:c.4064G>T	XP_011517019.1:p.Ser1355Ile
NM_017617.5:c.4763G>T MANE Select	NP_060087.3:p.Ser1588Ile
XM_011518717.2:c.4040G>T	XP_011517019.2:p.Ser1347Ile