Canonical Allele Identifier: CA1884231212

Gene: NOTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497220G= , CM000671.2:g.136497220G=	GRCh38
NC_000009.11:g.139391672G= , CM000671.1:g.139391672G=	GRCh37
NC_000009.10:g.138511493G=	NCBI36
NG_007458.1:g.53567C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6519C= MANE Select	ENSP00000498587.1:p.Ala2173=
ENST00000679595.1:c.*1559C=	ENSP00000506241.1:n.*1559C=
ENST00000679969.1:n.3115C=
ENST00000680003.1:n.2851C=
ENST00000680133.1:c.6405C=	ENSP00000505319.1:p.Ala2135=
ENST00000680218.1:c.6399C=	ENSP00000505339.1:p.Ala2133=
ENST00000680668.1:c.6405C=	ENSP00000506336.1:p.Ala2135=
ENST00000680778.1:c.4116C=	ENSP00000506033.1:p.Ala1372=
ENST00000680924.1:c.*3919C=	ENSP00000506031.1:n.*3919C=
ENST00000681135.1:c.*4128C=	ENSP00000506636.1:n.*4128C=
ENST00000681298.1:n.4624C=
ENST00000681454.1:c.*5755C=	ENSP00000505763.1:n.*5755C=
ENST00000277541.6:c.6519C=	ENSP00000277541.6:p.Ala2173=
NM_017617.3:c.6519C=	NP_060087.3:p.Ala2173=
XM_011518717.1:c.5820C=	XP_011517019.1:p.Ala1940=
NM_017617.5:c.6519C= MANE Select	NP_060087.3:p.Ala2173=
XM_011518717.2:c.5796C=	XP_011517019.2:p.Ala1932=