Canonical Allele Identifier: CA375631487

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133318266
• MyVariant Identifiers: chr9:g.139391692C>T (hg19) ; chr9:g.136497240C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497240C>T , CM000671.2:g.136497240C>T	GRCh38
NC_000009.11:g.139391692C>T , CM000671.1:g.139391692C>T	GRCh37
NC_000009.10:g.138511513C>T	NCBI36
NG_007458.1:g.53547G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6499G>A MANE Select	ENSP00000498587.1:p.Ala2167Thr
ENST00000679595.1:c.*1539G>A	ENSP00000506241.1:n.*1539G>A
ENST00000679969.1:n.3095G>A
ENST00000680003.1:n.2831G>A
ENST00000680133.1:c.6385G>A	ENSP00000505319.1:p.Ala2129Thr
ENST00000680218.1:c.6379G>A	ENSP00000505339.1:p.Ala2127Thr
ENST00000680668.1:c.6385G>A	ENSP00000506336.1:p.Ala2129Thr
ENST00000680778.1:c.4096G>A	ENSP00000506033.1:p.Ala1366Thr
ENST00000680924.1:c.*3899G>A	ENSP00000506031.1:n.*3899G>A
ENST00000681135.1:c.*4108G>A	ENSP00000506636.1:n.*4108G>A
ENST00000681298.1:n.4604G>A
ENST00000681454.1:c.*5735G>A	ENSP00000505763.1:n.*5735G>A
ENST00000277541.6:c.6499G>A	ENSP00000277541.6:p.Ala2167Thr
NM_017617.3:c.6499G>A	NP_060087.3:p.Ala2167Thr
XM_011518717.1:c.5800G>A	XP_011517019.1:p.Ala1934Thr
NM_017617.5:c.6499G>A MANE Select	NP_060087.3:p.Ala2167Thr
XM_011518717.2:c.5776G>A	XP_011517019.2:p.Ala1926Thr