Canonical Allele Identifier: CA341881313

Gene: NOTCH2

Linked Data

• MyVariant Identifiers: chr1:g.120510792T>G (hg19) ; chr1:g.119968169T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119968169T>G , CM000663.2:g.119968169T>G	GRCh38
NC_000001.10:g.120510792T>G , CM000663.1:g.120510792T>G	GRCh37
NC_000001.9:g.120312315T>G	NCBI36
NG_008163.1:g.106485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256646.7:c.1172A>C MANE Select	ENSP00000256646.2:p.Asp391Ala
ENST00000640021.1:c.392A>C	ENSP00000492223.1:n.392A>C
ENST00000256646.6:c.1172A>C	ENSP00000256646.2:p.Asp391Ala
ENST00000479412.2:n.1310A>C
ENST00000579475.7:c.1055A>C	ENSP00000477065.2:p.Asp352Ala
NM_001200001.1:c.1172A>C	NP_001186930.1:p.Asp391Ala
NM_024408.3:c.1172A>C	NP_077719.2:p.Asp391Ala
XM_005270901.2:c.1055A>C	XP_005270958.1:p.Asp352Ala
XM_011541519.1:c.1160A>C	XP_011539821.1:p.Asp387Ala
XM_011541520.1:c.1055A>C	XP_011539822.1:p.Asp352Ala
NM_024408.4:c.1172A>C MANE Select	NP_077719.2:p.Asp391Ala
NM_001200001.2:c.1172A>C	NP_001186930.1:p.Asp391Ala