Canonical Allele Identifier: CA375644986

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133336793
• MyVariant Identifiers: chr9:g.139399354T>A (hg19) ; chr9:g.136504902T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504902T>A , CM000671.2:g.136504902T>A	GRCh38
NC_000009.11:g.139399354T>A , CM000671.1:g.139399354T>A	GRCh37
NC_000009.10:g.138519175T>A	NCBI36
NG_007458.1:g.45885A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2596A>T
ENST00000651671.1:c.4789A>T MANE Select	ENSP00000498587.1:p.Ser1597Cys
ENST00000679595.1:c.4789A>T	ENSP00000506241.1:p.Ser1597Cys
ENST00000680133.1:c.4675A>T	ENSP00000505319.1:p.Ser1559Cys
ENST00000680218.1:c.4669A>T	ENSP00000505339.1:p.Ser1557Cys
ENST00000680668.1:c.4675A>T	ENSP00000506336.1:p.Ser1559Cys
ENST00000680778.1:c.2386A>T	ENSP00000506033.1:p.Ser796Cys
ENST00000680924.1:c.*2189A>T	ENSP00000506031.1:n.*2189A>T
ENST00000681135.1:c.*2398A>T	ENSP00000506636.1:n.*2398A>T
ENST00000681298.1:n.1602A>T
ENST00000681454.1:c.*4025A>T	ENSP00000505763.1:n.*4025A>T
ENST00000277541.6:c.4789A>T	ENSP00000277541.6:p.Ser1597Cys
NM_017617.3:c.4789A>T	NP_060087.3:p.Ser1597Cys
XM_011518717.1:c.4090A>T	XP_011517019.1:p.Ser1364Cys
NM_017617.5:c.4789A>T MANE Select	NP_060087.3:p.Ser1597Cys
XM_011518717.2:c.4066A>T	XP_011517019.2:p.Ser1356Cys