Canonical Allele Identifier: CA2863737

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15537014G>A , CM000666.2:g.15537014G>A	GRCh38
NC_000004.11:g.15538637G>A , CM000666.1:g.15538637G>A	GRCh37
NC_000004.10:g.15147735G>A	NCBI36
NG_013035.1:g.72149G>A , LRG_697:g.72149G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.1702G>A MANE Select	NP_001365544.1:p.Ala568Thr
ENST00000424120.6:c.1702G>A MANE Select	ENSP00000403465.1:p.Ala568Thr
NM_001080522.2:c.1702G>A , LRG_697t1:c.1702G>A	NP_001073991.2:p.Ala568Thr
NM_001378617.1:c.1555G>A	NP_001365546.1:p.Ala519Thr
ENST00000389652.11:c.1702G>A	ENSP00000374303.8:p.Ala568Thr
ENST00000389652.9:c.1164G>A
ENST00000424120.5:c.1702G>A	ENSP00000403465.1:p.Ala568Thr
ENST00000503292.5:c.1702G>A	ENSP00000421809.1:p.Ala568Thr
ENST00000503292.6:c.1702G>A	ENSP00000421809.1:p.Ala568Thr
ENST00000506643.4:c.30G>A
ENST00000506643.5:c.1555G>A	ENSP00000422931.2:p.Ala519Thr
ENST00000512702.5:c.1702G>A	ENSP00000422875.1:p.Ala568Thr
ENST00000512702.6:c.1702G>A	ENSP00000422875.2:p.Ala568Thr
ENST00000513811.5:n.1882G>A
ENST00000634028.1:c.1685G>A	ENSP00000488669.1:n.1685G>A
ENST00000634028.2:c.1555G>A	ENSP00000488669.2:p.Ala519Thr
ENST00000650860.2:c.1555G>A	ENSP00000498775.1:p.Ala519Thr
ENST00000651385.1:c.1555G>A	ENSP00000499005.1:p.Ala519Thr
ENST00000674945.1:c.1555G>A	ENSP00000502333.1:p.Ala519Thr
ENST00000676337.1:c.1555G>A	ENSP00000501728.1:p.Ala519Thr
XM_005248177.1:c.1702G>A	XP_005248234.1:p.Ala568Thr
XM_011513869.1:c.1702G>A	XP_011512171.1:p.Ala568Thr
XM_011513870.1:c.1702G>A	XP_011512172.1:p.Ala568Thr
XM_011513871.1:c.1555G>A	XP_011512173.1:p.Ala519Thr
XM_011513872.1:c.1702G>A	XP_011512174.1:p.Ala568Thr
XM_011513872.3:c.1702G>A	XP_011512174.1:p.Ala568Thr
XM_011513873.1:c.1702G>A	XP_011512175.1:p.Ala568Thr
XM_017008482.1:c.1555G>A	XP_016863971.1:p.Ala519Thr
XR_001741296.1:n.1902G>A