Canonical Allele Identifier: CA2603895851

Gene: NOTCH2

Linked Data

• gnomAD v3: 1-119975213-A-AT
• gnomAD v4: 1-119975213-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119975213_119975214insT , CM000663.2:g.119975213_119975214insT	GRCh38
NC_000001.10:g.120517836_120517837insT , CM000663.1:g.120517836_120517837insT	GRCh37
NC_000001.9:g.120319359_120319360insT	NCBI36
NG_008163.1:g.99440_99441insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256646.7:c.875-5470_875-5469insA MANE Select	ENSP00000256646.2:n.875-5470_875-5469insA
ENST00000640021.1:c.94+1136_94+1137insA	ENSP00000492223.1:n.94+1136_94+1137insA
ENST00000256646.6:c.875-5470_875-5469insA	ENSP00000256646.2:n.875-5470_875-5469insA
ENST00000479412.2:n.1013-5470_1013-5469insA
ENST00000579475.7:c.758-5470_758-5469insA	ENSP00000477065.2:n.758-5470_758-5469insA
NM_001200001.1:c.875-5470_875-5469insA	NP_001186930.1:n.875-5470_875-5469insA
NM_024408.3:c.875-5470_875-5469insA	NP_077719.2:n.875-5470_875-5469insA
XM_005270901.2:c.758-5470_758-5469insA	XP_005270958.1:n.758-5470_758-5469insA
XM_011541519.1:c.863-5470_863-5469insA	XP_011539821.1:n.863-5470_863-5469insA
XM_011541520.1:c.758-5470_758-5469insA	XP_011539822.1:n.758-5470_758-5469insA
NM_024408.4:c.875-5470_875-5469insA MANE Select	NP_077719.2:n.875-5470_875-5469insA
NM_001200001.2:c.875-5470_875-5469insA	NP_001186930.1:n.875-5470_875-5469insA