Canonical Allele Identifier: CA2864068

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15563394G>A , CM000666.2:g.15563394G>A	GRCh38
NC_000004.11:g.15565017G>A , CM000666.1:g.15565017G>A	GRCh37
NC_000004.10:g.15174115G>A	NCBI36
NG_013035.1:g.98529G>A , LRG_697:g.98529G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.3054G>A MANE Select	NP_001365544.1:p.Lys1018=
ENST00000424120.6:c.3054G>A MANE Select	ENSP00000403465.1:p.Lys1018=
NM_001080522.2:c.3054G>A , LRG_697t1:c.3054G>A	NP_001073991.2:p.Lys1018=
NM_001378617.1:c.2907G>A	NP_001365546.1:p.Lys969=
ENST00000389652.11:c.3069G>A	ENSP00000374303.8:p.Lys1023=
ENST00000389652.9:c.2531G>A
ENST00000424120.5:c.3054G>A	ENSP00000403465.1:p.Lys1018=
ENST00000503292.5:c.3054G>A	ENSP00000421809.1:p.Lys1018=
ENST00000503292.6:c.3054G>A	ENSP00000421809.1:p.Lys1018=
ENST00000506643.4:c.1382G>A
ENST00000506643.5:c.2907G>A	ENSP00000422931.2:p.Lys969=
ENST00000634028.1:c.3037G>A	ENSP00000488669.1:n.3037G>A
ENST00000634028.2:c.2907G>A	ENSP00000488669.2:p.Lys969=
ENST00000650860.2:c.*60G>A	ENSP00000498775.1:n.*60G>A
ENST00000674945.1:c.2907G>A	ENSP00000502333.1:p.Lys969=
ENST00000675619.1:n.3865G>A
ENST00000675768.1:n.274G>A
ENST00000676337.1:c.*60G>A	ENSP00000501728.1:n.*60G>A
ENST00000680586.1:n.3713G>A
XM_005248177.1:c.3054G>A	XP_005248234.1:p.Lys1018=
XM_011513869.1:c.3054G>A	XP_011512171.1:p.Lys1018=
XM_011513870.1:c.3054G>A	XP_011512172.1:p.Lys1018=
XM_011513871.1:c.2907G>A	XP_011512173.1:p.Lys969=
XM_011513872.1:c.*40G>A	XP_011512174.1:n.*40G>A
XM_011513872.3:c.*40G>A	XP_011512174.1:n.*40G>A
XM_017008482.1:c.2907G>A	XP_016863971.1:p.Lys969=
XR_001741296.1:n.3299G>A