Canonical Allele Identifier: CA375631879

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391817T>A (hg19) ; chr9:g.136497365T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497365T>A , CM000671.2:g.136497365T>A	GRCh38
NC_000009.11:g.139391817T>A , CM000671.1:g.139391817T>A	GRCh37
NC_000009.10:g.138511638T>A	NCBI36
NG_007458.1:g.53422A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6374A>T MANE Select	ENSP00000498587.1:p.His2125Leu
ENST00000679595.1:c.*1414A>T	ENSP00000506241.1:n.*1414A>T
ENST00000679969.1:n.2970A>T
ENST00000680003.1:n.2706A>T
ENST00000680133.1:c.6260A>T	ENSP00000505319.1:p.His2087Leu
ENST00000680218.1:c.6254A>T	ENSP00000505339.1:p.His2085Leu
ENST00000680668.1:c.6260A>T	ENSP00000506336.1:p.His2087Leu
ENST00000680778.1:c.3971A>T	ENSP00000506033.1:p.His1324Leu
ENST00000680924.1:c.*3774A>T	ENSP00000506031.1:n.*3774A>T
ENST00000681135.1:c.*3983A>T	ENSP00000506636.1:n.*3983A>T
ENST00000681298.1:n.4479A>T
ENST00000681454.1:c.*5610A>T	ENSP00000505763.1:n.*5610A>T
ENST00000277541.6:c.6374A>T	ENSP00000277541.6:p.His2125Leu
NM_017617.3:c.6374A>T	NP_060087.3:p.His2125Leu
XM_011518717.1:c.5675A>T	XP_011517019.1:p.His1892Leu
NM_017617.5:c.6374A>T MANE Select	NP_060087.3:p.His2125Leu
XM_011518717.2:c.5651A>T	XP_011517019.2:p.His1884Leu