Canonical Allele Identifier: CA375645730

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139399486C>A (hg19) ; chr9:g.136505034C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136505034C>A , CM000671.2:g.136505034C>A	GRCh38
NC_000009.11:g.139399486C>A , CM000671.1:g.139399486C>A	GRCh37
NC_000009.10:g.138519307C>A	NCBI36
NG_007458.1:g.45753G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2464G>T
ENST00000651671.1:c.4657G>T MANE Select	ENSP00000498587.1:p.Glu1553Ter
ENST00000679595.1:c.4657G>T	ENSP00000506241.1:p.Glu1553Ter
ENST00000680133.1:c.4543G>T	ENSP00000505319.1:p.Glu1515Ter
ENST00000680218.1:c.4537G>T	ENSP00000505339.1:p.Glu1513Ter
ENST00000680668.1:c.4543G>T	ENSP00000506336.1:p.Glu1515Ter
ENST00000680778.1:c.2254G>T	ENSP00000506033.1:p.Glu752Ter
ENST00000680924.1:c.*2057G>T	ENSP00000506031.1:n.*2057G>T
ENST00000681135.1:c.*2266G>T	ENSP00000506636.1:n.*2266G>T
ENST00000681298.1:n.1470G>T
ENST00000681454.1:c.*3893G>T	ENSP00000505763.1:n.*3893G>T
ENST00000277541.6:c.4657G>T	ENSP00000277541.6:p.Glu1553Ter
NM_017617.3:c.4657G>T	NP_060087.3:p.Glu1553Ter
XM_011518717.1:c.3958G>T	XP_011517019.1:p.Glu1320Ter
NM_017617.5:c.4657G>T MANE Select	NP_060087.3:p.Glu1553Ter
XM_011518717.2:c.3934G>T	XP_011517019.2:p.Glu1312Ter