Canonical Allele Identifier: CA375634387

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139393605A>T (hg19) ; chr9:g.136499153A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136499153A>T , CM000671.2:g.136499153A>T	GRCh38
NC_000009.11:g.139393605A>T , CM000671.1:g.139393605A>T	GRCh37
NC_000009.10:g.138513426A>T	NCBI36
NG_007458.1:g.51634T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6041T>A MANE Select	ENSP00000498587.1:p.Leu2014His
ENST00000679595.1:c.*1081T>A	ENSP00000506241.1:n.*1081T>A
ENST00000679969.1:n.2522T>A
ENST00000680003.1:n.2373T>A
ENST00000680133.1:c.5927T>A	ENSP00000505319.1:p.Leu1976His
ENST00000680218.1:c.5921T>A	ENSP00000505339.1:p.Leu1974His
ENST00000680668.1:c.5927T>A	ENSP00000506336.1:p.Leu1976His
ENST00000680778.1:c.3638T>A	ENSP00000506033.1:p.Leu1213His
ENST00000680924.1:c.*3441T>A	ENSP00000506031.1:n.*3441T>A
ENST00000681135.1:c.*3650T>A	ENSP00000506636.1:n.*3650T>A
ENST00000681298.1:n.4146T>A
ENST00000681454.1:c.*5277T>A	ENSP00000505763.1:n.*5277T>A
ENST00000277541.6:c.6041T>A	ENSP00000277541.6:p.Leu2014His
NM_017617.3:c.6041T>A	NP_060087.3:p.Leu2014His
XM_011518717.1:c.5342T>A	XP_011517019.1:p.Leu1781His
NM_017617.5:c.6041T>A MANE Select	NP_060087.3:p.Leu2014His
XM_011518717.2:c.5318T>A	XP_011517019.2:p.Leu1773His