Canonical Allele Identifier: CA356429685

Gene: CC2D2A

Linked Data

• MyVariant Identifiers: chr4:g.15591220A>G (hg19) ; chr4:g.15589597A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15589597A>G , CM000666.2:g.15589597A>G	GRCh38
NC_000004.11:g.15591220A>G , CM000666.1:g.15591220A>G	GRCh37
NC_000004.10:g.15200318A>G	NCBI36
NG_013035.1:g.124732A>G , LRG_697:g.124732A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.4268A>G	ENSP00000374303.8:p.Asn1423Ser
ENST00000424120.6:c.4232A>G MANE Select	ENSP00000403465.1:p.Asn1411Ser
ENST00000503292.6:c.4232A>G	ENSP00000421809.1:p.Asn1411Ser
ENST00000506643.5:c.4085A>G	ENSP00000422931.2:p.Asn1362Ser
ENST00000514039.6:c.461A>G	ENSP00000488534.2:p.Asn154Ser
ENST00000634028.2:c.4085A>G	ENSP00000488669.2:p.Asn1362Ser
ENST00000650860.2:c.*1729A>G	ENSP00000498775.1:n.*1729A>G
ENST00000674945.1:c.3908A>G	ENSP00000502333.1:p.Asn1303Ser
ENST00000675768.1:n.1452A>G
ENST00000680586.1:n.4891A>G
ENST00000389652.9:c.3730A>G
ENST00000424120.5:c.4232A>G	ENSP00000403465.1:p.Asn1411Ser
ENST00000503292.5:c.4232A>G	ENSP00000421809.1:p.Asn1411Ser
ENST00000506643.4:c.2560A>G
ENST00000634028.1:c.4038A>G	ENSP00000488669.1:n.4038A>G
NM_001080522.2:c.4232A>G , LRG_697t1:c.4232A>G	NP_001073991.2:p.Asn1411Ser
XM_005248177.1:c.4232A>G	XP_005248234.1:p.Asn1411Ser
XM_011513869.1:c.4250A>G	XP_011512171.1:p.Asn1417Ser
XM_011513870.1:c.4250A>G	XP_011512172.1:p.Asn1417Ser
XM_011513871.1:c.4103A>G	XP_011512173.1:p.Asn1368Ser
XM_017008482.1:c.4085A>G	XP_016863971.1:p.Asn1362Ser
NM_001378615.1:c.4232A>G MANE Select	NP_001365544.1:p.Asn1411Ser
NM_001378617.1:c.4085A>G	NP_001365546.1:p.Asn1362Ser