Canonical Allele Identifier: CA1884231154

Gene: NOTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497162T= , CM000671.2:g.136497162T=	GRCh38
NC_000009.11:g.139391614T= , CM000671.1:g.139391614T=	GRCh37
NC_000009.10:g.138511435T=	NCBI36
NG_007458.1:g.53625A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6577A= MANE Select	ENSP00000498587.1:p.Ser2193=
ENST00000679595.1:c.*1617A=	ENSP00000506241.1:n.*1617A=
ENST00000679969.1:n.3173A=
ENST00000680003.1:n.2909A=
ENST00000680133.1:c.6463A=	ENSP00000505319.1:p.Ser2155=
ENST00000680218.1:c.6457A=	ENSP00000505339.1:p.Ser2153=
ENST00000680668.1:c.6463A=	ENSP00000506336.1:p.Ser2155=
ENST00000680778.1:c.4174A=	ENSP00000506033.1:p.Ser1392=
ENST00000680924.1:c.*3977A=	ENSP00000506031.1:n.*3977A=
ENST00000681135.1:c.*4186A=	ENSP00000506636.1:n.*4186A=
ENST00000681298.1:n.4682A=
ENST00000681454.1:c.*5813A=	ENSP00000505763.1:n.*5813A=
ENST00000277541.6:c.6577A=	ENSP00000277541.6:p.Ser2193=
NM_017617.3:c.6577A=	NP_060087.3:p.Ser2193=
XM_011518717.1:c.5878A=	XP_011517019.1:p.Ser1960=
NM_017617.5:c.6577A= MANE Select	NP_060087.3:p.Ser2193=
XM_011518717.2:c.5854A=	XP_011517019.2:p.Ser1952=