Canonical Allele Identifier: CA375634297

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133322594
• MyVariant Identifiers: chr9:g.139393584A>G (hg19) ; chr9:g.136499132A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136499132A>G , CM000671.2:g.136499132A>G	GRCh38
NC_000009.11:g.139393584A>G , CM000671.1:g.139393584A>G	GRCh37
NC_000009.10:g.138513405A>G	NCBI36
NG_007458.1:g.51655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6062T>C MANE Select	ENSP00000498587.1:p.Val2021Ala
ENST00000679595.1:c.*1102T>C	ENSP00000506241.1:n.*1102T>C
ENST00000679969.1:n.2543T>C
ENST00000680003.1:n.2394T>C
ENST00000680133.1:c.5948T>C	ENSP00000505319.1:p.Val1983Ala
ENST00000680218.1:c.5942T>C	ENSP00000505339.1:p.Val1981Ala
ENST00000680668.1:c.5948T>C	ENSP00000506336.1:p.Val1983Ala
ENST00000680778.1:c.3659T>C	ENSP00000506033.1:p.Val1220Ala
ENST00000680924.1:c.*3462T>C	ENSP00000506031.1:n.*3462T>C
ENST00000681135.1:c.*3671T>C	ENSP00000506636.1:n.*3671T>C
ENST00000681298.1:n.4167T>C
ENST00000681454.1:c.*5298T>C	ENSP00000505763.1:n.*5298T>C
ENST00000277541.6:c.6062T>C	ENSP00000277541.6:p.Val2021Ala
NM_017617.3:c.6062T>C	NP_060087.3:p.Val2021Ala
XM_011518717.1:c.5363T>C	XP_011517019.1:p.Val1788Ala
NM_017617.5:c.6062T>C MANE Select	NP_060087.3:p.Val2021Ala
XM_011518717.2:c.5339T>C	XP_011517019.2:p.Val1780Ala