Canonical Allele Identifier: CA375644031

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133335701
• MyVariant Identifiers: chr9:g.139399142G>C (hg19) ; chr9:g.136504690G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504690G>C , CM000671.2:g.136504690G>C	GRCh38
NC_000009.11:g.139399142G>C , CM000671.1:g.139399142G>C	GRCh37
NC_000009.10:g.138518963G>C	NCBI36
NG_007458.1:g.46097C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000645828.1:n.2808C>G
ENST00000651671.1:c.5001C>G MANE Select	ENSP00000498587.1:p.Asp1667Glu
ENST00000679595.1:c.5001C>G	ENSP00000506241.1:p.Asp1667Glu
ENST00000680133.1:c.4887C>G	ENSP00000505319.1:p.Asp1629Glu
ENST00000680218.1:c.4881C>G	ENSP00000505339.1:p.Asp1627Glu
ENST00000680668.1:c.4887C>G	ENSP00000506336.1:p.Asp1629Glu
ENST00000680778.1:c.2598C>G	ENSP00000506033.1:p.Asp866Glu
ENST00000680924.1:c.*2401C>G	ENSP00000506031.1:n.*2401C>G
ENST00000681135.1:c.*2610C>G	ENSP00000506636.1:n.*2610C>G
ENST00000681298.1:n.1814C>G
ENST00000681454.1:c.*4237C>G	ENSP00000505763.1:n.*4237C>G
ENST00000277541.6:c.5001C>G	ENSP00000277541.6:p.Asp1667Glu
ENST00000494783.1:n.156C>G
NM_017617.3:c.5001C>G	NP_060087.3:p.Asp1667Glu
XM_011518717.1:c.4302C>G	XP_011517019.1:p.Asp1434Glu
NM_017617.5:c.5001C>G MANE Select	NP_060087.3:p.Asp1667Glu
XM_011518717.2:c.4278C>G	XP_011517019.2:p.Asp1426Glu