Canonical Allele Identifier: CA375645089

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139399374A>C (hg19) ; chr9:g.136504922A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504922A>C , CM000671.2:g.136504922A>C	GRCh38
NC_000009.11:g.139399374A>C , CM000671.1:g.139399374A>C	GRCh37
NC_000009.10:g.138519195A>C	NCBI36
NG_007458.1:g.45865T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2576T>G
ENST00000651671.1:c.4769T>G MANE Select	ENSP00000498587.1:p.Phe1590Cys
ENST00000679595.1:c.4769T>G	ENSP00000506241.1:p.Phe1590Cys
ENST00000680133.1:c.4655T>G	ENSP00000505319.1:p.Phe1552Cys
ENST00000680218.1:c.4649T>G	ENSP00000505339.1:p.Phe1550Cys
ENST00000680668.1:c.4655T>G	ENSP00000506336.1:p.Phe1552Cys
ENST00000680778.1:c.2366T>G	ENSP00000506033.1:p.Phe789Cys
ENST00000680924.1:c.*2169T>G	ENSP00000506031.1:n.*2169T>G
ENST00000681135.1:c.*2378T>G	ENSP00000506636.1:n.*2378T>G
ENST00000681298.1:n.1582T>G
ENST00000681454.1:c.*4005T>G	ENSP00000505763.1:n.*4005T>G
ENST00000277541.6:c.4769T>G	ENSP00000277541.6:p.Phe1590Cys
NM_017617.3:c.4769T>G	NP_060087.3:p.Phe1590Cys
XM_011518717.1:c.4070T>G	XP_011517019.1:p.Phe1357Cys
NM_017617.5:c.4769T>G MANE Select	NP_060087.3:p.Phe1590Cys
XM_011518717.2:c.4046T>G	XP_011517019.2:p.Phe1349Cys