Canonical Allele Identifier: CA375633970

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133321726
• MyVariant Identifiers: chr9:g.139393404C>T (hg19) ; chr9:g.136498952C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136498952C>T , CM000671.2:g.136498952C>T	GRCh38
NC_000009.11:g.139393404C>T , CM000671.1:g.139393404C>T	GRCh37
NC_000009.10:g.138513225C>T	NCBI36
NG_007458.1:g.51835G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6127G>A MANE Select	ENSP00000498587.1:p.Ala2043Thr
ENST00000679595.1:c.*1167G>A	ENSP00000506241.1:n.*1167G>A
ENST00000679969.1:n.2723G>A
ENST00000680003.1:n.2459G>A
ENST00000680133.1:c.6013G>A	ENSP00000505319.1:p.Ala2005Thr
ENST00000680218.1:c.6007G>A	ENSP00000505339.1:p.Ala2003Thr
ENST00000680668.1:c.6013G>A	ENSP00000506336.1:p.Ala2005Thr
ENST00000680778.1:c.3724G>A	ENSP00000506033.1:p.Ala1242Thr
ENST00000680924.1:c.*3527G>A	ENSP00000506031.1:n.*3527G>A
ENST00000681135.1:c.*3736G>A	ENSP00000506636.1:n.*3736G>A
ENST00000681298.1:n.4232G>A
ENST00000681454.1:c.*5363G>A	ENSP00000505763.1:n.*5363G>A
ENST00000277541.6:c.6127G>A	ENSP00000277541.6:p.Ala2043Thr
NM_017617.3:c.6127G>A	NP_060087.3:p.Ala2043Thr
XM_011518717.1:c.5428G>A	XP_011517019.1:p.Ala1810Thr
NM_017617.5:c.6127G>A MANE Select	NP_060087.3:p.Ala2043Thr
XM_011518717.2:c.5404G>A	XP_011517019.2:p.Ala1802Thr