Canonical Allele Identifier: CA375645020

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139399359T>G (hg19) ; chr9:g.136504907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504907T>G , CM000671.2:g.136504907T>G	GRCh38
NC_000009.11:g.139399359T>G , CM000671.1:g.139399359T>G	GRCh37
NC_000009.10:g.138519180T>G	NCBI36
NG_007458.1:g.45880A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2591A>C
ENST00000651671.1:c.4784A>C MANE Select	ENSP00000498587.1:p.Glu1595Ala
ENST00000679595.1:c.4784A>C	ENSP00000506241.1:p.Glu1595Ala
ENST00000680133.1:c.4670A>C	ENSP00000505319.1:p.Glu1557Ala
ENST00000680218.1:c.4664A>C	ENSP00000505339.1:p.Glu1555Ala
ENST00000680668.1:c.4670A>C	ENSP00000506336.1:p.Glu1557Ala
ENST00000680778.1:c.2381A>C	ENSP00000506033.1:p.Glu794Ala
ENST00000680924.1:c.*2184A>C	ENSP00000506031.1:n.*2184A>C
ENST00000681135.1:c.*2393A>C	ENSP00000506636.1:n.*2393A>C
ENST00000681298.1:n.1597A>C
ENST00000681454.1:c.*4020A>C	ENSP00000505763.1:n.*4020A>C
ENST00000277541.6:c.4784A>C	ENSP00000277541.6:p.Glu1595Ala
NM_017617.3:c.4784A>C	NP_060087.3:p.Glu1595Ala
XM_011518717.1:c.4085A>C	XP_011517019.1:p.Glu1362Ala
NM_017617.5:c.4784A>C MANE Select	NP_060087.3:p.Glu1595Ala
XM_011518717.2:c.4061A>C	XP_011517019.2:p.Glu1354Ala