Canonical Allele Identifier: CA375633670

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133321439
• MyVariant Identifiers: chr9:g.139393355T>G (hg19) ; chr9:g.136498903T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136498903T>G , CM000671.2:g.136498903T>G	GRCh38
NC_000009.11:g.139393355T>G , CM000671.1:g.139393355T>G	GRCh37
NC_000009.10:g.138513176T>G	NCBI36
NG_007458.1:g.51884A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6176A>C MANE Select	ENSP00000498587.1:p.Asn2059Thr
ENST00000679595.1:c.*1216A>C	ENSP00000506241.1:n.*1216A>C
ENST00000679969.1:n.2772A>C
ENST00000680003.1:n.2508A>C
ENST00000680133.1:c.6062A>C	ENSP00000505319.1:p.Asn2021Thr
ENST00000680218.1:c.6056A>C	ENSP00000505339.1:p.Asn2019Thr
ENST00000680668.1:c.6062A>C	ENSP00000506336.1:p.Asn2021Thr
ENST00000680778.1:c.3773A>C	ENSP00000506033.1:p.Asn1258Thr
ENST00000680924.1:c.*3576A>C	ENSP00000506031.1:n.*3576A>C
ENST00000681135.1:c.*3785A>C	ENSP00000506636.1:n.*3785A>C
ENST00000681298.1:n.4281A>C
ENST00000681454.1:c.*5412A>C	ENSP00000505763.1:n.*5412A>C
ENST00000277541.6:c.6176A>C	ENSP00000277541.6:p.Asn2059Thr
NM_017617.3:c.6176A>C	NP_060087.3:p.Asn2059Thr
XM_011518717.1:c.5477A>C	XP_011517019.1:p.Asn1826Thr
NM_017617.5:c.6176A>C MANE Select	NP_060087.3:p.Asn2059Thr
XM_011518717.2:c.5453A>C	XP_011517019.2:p.Asn1818Thr