Canonical Allele Identifier: CA1259712519

Gene: ADD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70747668G= , CM000664.2:g.70747668G=	GRCh38
NC_000002.11:g.70974800G= , CM000664.1:g.70974800G=	GRCh37
NC_000002.10:g.70828308G=	NCBI36
NG_029481.1:g.25576C=
NG_029481.2:g.25576C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264436.9:c.-154+20218C= MANE Select	ENSP00000264436.3:n.-154+20218C=
ENST00000264436.8:c.-154+20218C=	ENSP00000264436.3:n.-154+20218C=
ENST00000355733.7:c.-154+20218C=	ENSP00000347972.3:n.-154+20218C=
ENST00000403045.6:c.-154+20218C=	ENSP00000384303.2:n.-154+20218C=
ENST00000407644.6:c.-154+19936C=	ENSP00000384677.2:n.-154+19936C=
ENST00000413157.6:c.-154+20218C=	ENSP00000388072.2:n.-154+20218C=
ENST00000425976.5:c.-154+19662C=	ENSP00000412681.1:n.-154+19662C=
ENST00000430656.5:c.14+20218C=	ENSP00000398112.1:n.14+20218C=
ENST00000447731.6:c.-219-6262C=	ENSP00000403722.1:n.-219-6262C=
ENST00000473232.1:n.315+20218C=
ENST00000496178.1:n.436+12938C=
NM_001185054.1:c.-154+19936C=	NP_001171983.1:n.-154+19936C=
NM_001185055.1:c.14+20218C=	NP_001171984.1:n.14+20218C=
NM_001617.3:c.-154+20218C=	NP_001608.1:n.-154+20218C=
NM_017482.3:c.-154+20218C=	NP_059516.2:n.-154+20218C=
NM_017488.3:c.-154+20218C=	NP_059522.1:n.-154+20218C=
XM_011532503.1:c.-272+20218C=	XP_011530805.1:n.-272+20218C=
NM_001617.4:c.-154+20218C= MANE Select	NP_001608.1:n.-154+20218C=
NM_001185055.2:c.14+20218C=	NP_001171984.1:n.14+20218C=
NM_017482.4:c.-154+20218C=	NP_059516.2:n.-154+20218C=
NM_017488.4:c.-154+20218C=	NP_059522.1:n.-154+20218C=
NM_001185054.2:c.-154+19936C=	NP_001171983.1:n.-154+19936C=