Canonical Allele Identifier: CA356431491

Gene: CC2D2A

Linked Data

• MyVariant Identifiers: chr4:g.15597736C>A (hg19) ; chr4:g.15596113C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15596113C>A , CM000666.2:g.15596113C>A	GRCh38
NC_000004.11:g.15597736C>A , CM000666.1:g.15597736C>A	GRCh37
NC_000004.10:g.15206834C>A	NCBI36
NG_013035.1:g.131248C>A , LRG_697:g.131248C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.4379C>A	ENSP00000374303.8:p.Ser1460Tyr
ENST00000424120.6:c.4343C>A MANE Select	ENSP00000403465.1:p.Ser1448Tyr
ENST00000503292.6:c.4343C>A	ENSP00000421809.1:p.Ser1448Tyr
ENST00000506643.5:c.4196C>A	ENSP00000422931.2:p.Ser1399Tyr
ENST00000513035.2:n.242C>A
ENST00000514039.6:c.544-1294C>A	ENSP00000488534.2:n.544-1294C>A
ENST00000634028.2:c.4168-31C>A	ENSP00000488669.2:n.4168-31C>A
ENST00000650860.2:c.*1840C>A	ENSP00000498775.1:n.*1840C>A
ENST00000674945.1:c.4019C>A	ENSP00000502333.1:p.Ser1340Tyr
ENST00000680586.1:n.5002C>A
ENST00000389652.9:c.3841C>A
ENST00000424120.5:c.4343C>A	ENSP00000403465.1:p.Ser1448Tyr
ENST00000503292.5:c.4343C>A	ENSP00000421809.1:p.Ser1448Tyr
ENST00000506643.4:c.2643-31C>A
ENST00000513035.1:n.242C>A
ENST00000514039.5:c.54-1294C>A
ENST00000634028.1:c.4149C>A	ENSP00000488669.1:n.4149C>A
NM_001080522.2:c.4343C>A , LRG_697t1:c.4343C>A	NP_001073991.2:p.Ser1448Tyr
XM_005248177.1:c.4343C>A	XP_005248234.1:p.Ser1448Tyr
XM_011513869.1:c.4361C>A	XP_011512171.1:p.Ser1454Tyr
XM_011513870.1:c.4361C>A	XP_011512172.1:p.Ser1454Tyr
XM_011513871.1:c.4214C>A	XP_011512173.1:p.Ser1405Tyr
XM_017008482.1:c.4196C>A	XP_016863971.1:p.Ser1399Tyr
NM_001378615.1:c.4343C>A MANE Select	NP_001365544.1:p.Ser1448Tyr
NM_001378617.1:c.4196C>A	NP_001365546.1:p.Ser1399Tyr