Canonical Allele Identifier: CA420038913

Gene: NOTCH2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119968228G>C , CM000663.2:g.119968228G>C	GRCh38
NC_000001.10:g.120510851G>C , CM000663.1:g.120510851G>C	GRCh37
NC_000001.9:g.120312374G>C	NCBI36
NG_008163.1:g.106426C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024408.4:c.1113C>G MANE Select	NP_077719.2:p.Leu371=
ENST00000256646.7:c.1113C>G MANE Select	ENSP00000256646.2:p.Leu371=
NM_001200001.1:c.1113C>G	NP_001186930.1:p.Leu371=
NM_001200001.2:c.1113C>G	NP_001186930.1:p.Leu371=
NM_024408.3:c.1113C>G	NP_077719.2:p.Leu371=
ENST00000256646.6:c.1113C>G	ENSP00000256646.2:p.Leu371=
ENST00000479412.2:n.1251C>G
ENST00000579475.7:c.996C>G	ENSP00000477065.2:p.Leu332=
ENST00000640021.1:c.333C>G	ENSP00000492223.1:n.333C>G
XM_005270901.2:c.996C>G	XP_005270958.1:p.Leu332=
XM_011541519.1:c.1101C>G	XP_011539821.1:p.Leu367=
XM_011541520.1:c.996C>G	XP_011539822.1:p.Leu332=