Canonical Allele Identifier: CA1141189145

Gene: NOTCH2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119967555C= , CM000663.2:g.119967555C=	GRCh38
NC_000001.10:g.120510178C= , CM000663.1:g.120510178C=	GRCh37
NC_000001.9:g.120311701C=	NCBI36
NG_008163.1:g.107099G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256646.7:c.1331G= MANE Select	ENSP00000256646.2:p.Cys444=
ENST00000640021.1:c.551G=	ENSP00000492223.1:n.551G=
ENST00000256646.6:c.1331G=	ENSP00000256646.2:p.Cys444=
ENST00000479412.2:n.1469G=
ENST00000579475.7:c.1214G=	ENSP00000477065.2:p.Cys405=
NM_001200001.1:c.1331G=	NP_001186930.1:p.Cys444=
NM_024408.3:c.1331G=	NP_077719.2:p.Cys444=
XM_005270901.2:c.1214G=	XP_005270958.1:p.Cys405=
XM_011541519.1:c.1319G=	XP_011539821.1:p.Cys440=
XM_011541520.1:c.1214G=	XP_011539822.1:p.Cys405=
NM_024408.4:c.1331G= MANE Select	NP_077719.2:p.Cys444=
NM_001200001.2:c.1331G=	NP_001186930.1:p.Cys444=