Canonical Allele Identifier: CA356432106

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15597424C>A , CM000666.2:g.15597424C>A	GRCh38
NC_000004.11:g.15599047C>A , CM000666.1:g.15599047C>A	GRCh37
NC_000004.10:g.15208145C>A	NCBI36
NG_013035.1:g.132559C>A , LRG_697:g.132559C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.4455C>A MANE Select	NP_001365544.1:p.Tyr1485Ter
ENST00000424120.6:c.4455C>A MANE Select	ENSP00000403465.1:p.Tyr1485Ter
NM_001080522.2:c.4455C>A , LRG_697t1:c.4455C>A	NP_001073991.2:p.Tyr1485Ter
NM_001378617.1:c.4308C>A	NP_001365546.1:p.Tyr1436Ter
ENST00000389652.11:c.4491C>A	ENSP00000374303.8:p.Tyr1497Ter
ENST00000389652.9:c.3953C>A
ENST00000424120.5:c.4455C>A	ENSP00000403465.1:p.Tyr1485Ter
ENST00000503292.5:c.4455C>A	ENSP00000421809.1:p.Tyr1485Ter
ENST00000503292.6:c.4455C>A	ENSP00000421809.1:p.Tyr1485Ter
ENST00000506643.4:c.2724C>A
ENST00000506643.5:c.4308C>A	ENSP00000422931.2:p.Tyr1436Ter
ENST00000513035.1:n.354C>A
ENST00000513035.2:n.354C>A
ENST00000514039.5:c.71C>A
ENST00000514039.6:c.561C>A	ENSP00000488534.2:p.Tyr187Ter
ENST00000634028.1:c.4261C>A	ENSP00000488669.1:n.4261C>A
ENST00000634028.2:c.4249C>A	ENSP00000488669.2:n.4249C>A
ENST00000650860.2:c.*1952C>A	ENSP00000498775.1:n.*1952C>A
ENST00000674945.1:c.4131C>A	ENSP00000502333.1:p.Tyr1377Ter
ENST00000680586.1:n.5114C>A
XM_005248177.1:c.4455C>A	XP_005248234.1:p.Tyr1485Ter
XM_011513869.1:c.4473C>A	XP_011512171.1:p.Tyr1491Ter
XM_011513870.1:c.4473C>A	XP_011512172.1:p.Tyr1491Ter
XM_011513871.1:c.4326C>A	XP_011512173.1:p.Tyr1442Ter
XM_017008482.1:c.4308C>A	XP_016863971.1:p.Tyr1436Ter