Canonical Allele Identifier: CA1192534908

Gene: NOTCH2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119975149_119975152delinsAAAG , CM000663.2:g.119975149_119975152delinsAAAG	GRCh38
NC_000001.10:g.120517772_120517775delinsAAAG , CM000663.1:g.120517772_120517775delinsAAAG	GRCh37
NC_000001.9:g.120319295_120319298delinsAAAG	NCBI36
NG_008163.1:g.99502_99505delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256646.7:c.875-5408_875-5405delinsCTTT MANE Select	ENSP00000256646.2:n.875-5408_875-5405delinsCTTT
ENST00000640021.1:c.94+1198_94+1201delinsCTTT	ENSP00000492223.1:n.94+1198_94+1201delinsCTTT
ENST00000256646.6:c.875-5408_875-5405delinsCTTT	ENSP00000256646.2:n.875-5408_875-5405delinsCTTT
ENST00000479412.2:n.1013-5408_1013-5405delinsCTTT
ENST00000579475.7:c.758-5408_758-5405delinsCTTT	ENSP00000477065.2:n.758-5408_758-5405delinsCTTT
NM_001200001.1:c.875-5408_875-5405delinsCTTT	NP_001186930.1:n.875-5408_875-5405delinsCTTT
NM_024408.3:c.875-5408_875-5405delinsCTTT	NP_077719.2:n.875-5408_875-5405delinsCTTT
XM_005270901.2:c.758-5408_758-5405delinsCTTT	XP_005270958.1:n.758-5408_758-5405delinsCTTT
XM_011541519.1:c.863-5408_863-5405delinsCTTT	XP_011539821.1:n.863-5408_863-5405delinsCTTT
XM_011541520.1:c.758-5408_758-5405delinsCTTT	XP_011539822.1:n.758-5408_758-5405delinsCTTT
NM_024408.4:c.875-5408_875-5405delinsCTTT MANE Select	NP_077719.2:n.875-5408_875-5405delinsCTTT
NM_001200001.2:c.875-5408_875-5405delinsCTTT	NP_001186930.1:n.875-5408_875-5405delinsCTTT