Canonical Allele Identifier: CA1259679122

Gene: ADD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70673271G= , CM000664.2:g.70673271G=	GRCh38
NC_000002.11:g.70900403G= , CM000664.1:g.70900403G=	GRCh37
NC_000002.10:g.70753911G=	NCBI36
NG_029481.1:g.99973C=
NG_029481.2:g.99973C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001617.4:c.1742-265C= MANE Select	NP_001608.1:n.1742-265C=
ENST00000264436.9:c.1742-265C= MANE Select	ENSP00000264436.3:n.1742-265C=
NM_001185054.1:c.1742-265C=	NP_001171983.1:n.1742-265C=
NM_001185054.2:c.1742-265C=	NP_001171983.1:n.1742-265C=
NM_001617.3:c.1742-265C=	NP_001608.1:n.1742-265C=
NM_017488.3:c.1797C=	NP_059522.1:p.Ser599=
NM_017488.4:c.1797C=	NP_059522.1:p.Ser599=
ENST00000264436.8:c.1742-265C=	ENSP00000264436.3:n.1742-265C=
ENST00000355733.7:c.1797C=	ENSP00000347972.3:p.Ser599=
ENST00000403045.6:c.1742-265C=	ENSP00000384303.2:n.1742-265C=
ENST00000407644.6:c.1742-265C=	ENSP00000384677.2:n.1742-265C=
ENST00000481675.1:n.78C=
XM_011532502.1:c.1742-265C=	XP_011530804.1:n.1742-265C=
XM_011532502.2:c.1742-265C=	XP_011530804.1:n.1742-265C=
XM_011532503.1:c.1742-265C=	XP_011530805.1:n.1742-265C=
XR_940230.2:n.30G=