Canonical Allele Identifier: CA356434128

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15599614C>A , CM000666.2:g.15599614C>A	GRCh38
NC_000004.11:g.15601237C>A , CM000666.1:g.15601237C>A	GRCh37
NC_000004.10:g.15210335C>A	NCBI36
NG_013035.1:g.134749C>A , LRG_697:g.134749C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.4582C>A MANE Select	NP_001365544.1:p.Arg1528Ser
ENST00000424120.6:c.4582C>A MANE Select	ENSP00000403465.1:p.Arg1528Ser
NM_001080522.2:c.4582C>A , LRG_697t1:c.4582C>A	NP_001073991.2:p.Arg1528Ser
NM_001378617.1:c.4435C>A	NP_001365546.1:p.Arg1479Ser
ENST00000389652.11:c.4618C>A	ENSP00000374303.8:p.Arg1540Ser
ENST00000389652.9:c.4080C>A
ENST00000424120.5:c.4582C>A	ENSP00000403465.1:p.Arg1528Ser
ENST00000503292.5:c.4582C>A	ENSP00000421809.1:p.Arg1528Ser
ENST00000503292.6:c.4582C>A	ENSP00000421809.1:p.Arg1528Ser
ENST00000506643.4:c.2851C>A
ENST00000506643.5:c.4435C>A	ENSP00000422931.2:p.Arg1479Ser
ENST00000514039.5:c.198C>A
ENST00000514039.6:c.688C>A	ENSP00000488534.2:p.Arg230Ser
ENST00000634028.1:c.4388C>A	ENSP00000488669.1:n.4388C>A
ENST00000634028.2:c.4376C>A	ENSP00000488669.2:n.4376C>A
ENST00000650860.2:c.*2079C>A	ENSP00000498775.1:n.*2079C>A
ENST00000674945.1:c.4258C>A	ENSP00000502333.1:p.Arg1420Ser
ENST00000680586.1:n.5241C>A
XM_005248177.1:c.4582C>A	XP_005248234.1:p.Arg1528Ser
XM_011513869.1:c.4600C>A	XP_011512171.1:p.Arg1534Ser
XM_011513870.1:c.4600C>A	XP_011512172.1:p.Arg1534Ser
XM_011513871.1:c.4453C>A	XP_011512173.1:p.Arg1485Ser
XM_017008482.1:c.4435C>A	XP_016863971.1:p.Arg1479Ser