Canonical Allele Identifier: CA1884231267

Gene: NOTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497274G= , CM000671.2:g.136497274G=	GRCh38
NC_000009.11:g.139391726G= , CM000671.1:g.139391726G=	GRCh37
NC_000009.10:g.138511547G=	NCBI36
NG_007458.1:g.53513C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6465C= MANE Select	ENSP00000498587.1:p.Gly2155=
ENST00000679595.1:c.*1505C=	ENSP00000506241.1:n.*1505C=
ENST00000679969.1:n.3061C=
ENST00000680003.1:n.2797C=
ENST00000680133.1:c.6351C=	ENSP00000505319.1:p.Gly2117=
ENST00000680218.1:c.6345C=	ENSP00000505339.1:p.Gly2115=
ENST00000680668.1:c.6351C=	ENSP00000506336.1:p.Gly2117=
ENST00000680778.1:c.4062C=	ENSP00000506033.1:p.Gly1354=
ENST00000680924.1:c.*3865C=	ENSP00000506031.1:n.*3865C=
ENST00000681135.1:c.*4074C=	ENSP00000506636.1:n.*4074C=
ENST00000681298.1:n.4570C=
ENST00000681454.1:c.*5701C=	ENSP00000505763.1:n.*5701C=
ENST00000277541.6:c.6465C=	ENSP00000277541.6:p.Gly2155=
NM_017617.3:c.6465C=	NP_060087.3:p.Gly2155=
XM_011518717.1:c.5766C=	XP_011517019.1:p.Gly1922=
NM_017617.5:c.6465C= MANE Select	NP_060087.3:p.Gly2155=
XM_011518717.2:c.5742C=	XP_011517019.2:p.Gly1914=