Canonical Allele Identifier: CA2864481

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15601348G>A , CM000666.2:g.15601348G>A	GRCh38
NC_000004.11:g.15602971G>A , CM000666.1:g.15602971G>A	GRCh37
NC_000004.10:g.15212069G>A	NCBI36
NG_013035.1:g.136483G>A , LRG_697:g.136483G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.4786G>A MANE Select	NP_001365544.1:p.Ala1596Thr
ENST00000424120.6:c.4786G>A MANE Select	ENSP00000403465.1:p.Ala1596Thr
NM_001080522.2:c.4786G>A , LRG_697t1:c.4786G>A	NP_001073991.2:p.Ala1596Thr
NM_001378617.1:c.4639G>A	NP_001365546.1:p.Ala1547Thr
ENST00000389652.11:c.4822G>A	ENSP00000374303.8:p.Ala1608Thr
ENST00000389652.9:c.4284G>A
ENST00000424120.5:c.4786G>A	ENSP00000403465.1:p.Ala1596Thr
ENST00000503292.5:c.4786G>A	ENSP00000421809.1:p.Ala1596Thr
ENST00000503292.6:c.4786G>A	ENSP00000421809.1:p.Ala1596Thr
ENST00000506643.4:c.3055G>A
ENST00000506643.5:c.4639G>A	ENSP00000422931.2:p.Ala1547Thr
ENST00000514039.5:c.402G>A
ENST00000514039.6:c.892G>A	ENSP00000488534.2:p.Ala298Thr
ENST00000634028.1:c.4592G>A	ENSP00000488669.1:n.4592G>A
ENST00000634028.2:c.4580G>A	ENSP00000488669.2:n.4580G>A
ENST00000650860.2:c.*2283G>A	ENSP00000498775.1:n.*2283G>A
ENST00000674945.1:c.4462G>A	ENSP00000502333.1:p.Ala1488Thr
XM_005248177.1:c.4786G>A	XP_005248234.1:p.Ala1596Thr
XM_011513869.1:c.4804G>A	XP_011512171.1:p.Ala1602Thr
XM_011513870.1:c.4804G>A	XP_011512172.1:p.Ala1602Thr
XM_011513871.1:c.4657G>A	XP_011512173.1:p.Ala1553Thr
XM_017008482.1:c.4639G>A	XP_016863971.1:p.Ala1547Thr