Canonical Allele Identifier: CA438390946

Gene: CC2D2A

Linked Data

• MyVariant Identifiers: chr4:g.15591191T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15589568T>A , CM000666.2:g.15589568T>A	GRCh38
NC_000004.11:g.15591191T>A , CM000666.1:g.15591191T>A	GRCh37
NC_000004.10:g.15200289T>A	NCBI36
NG_013035.1:g.124703T>A , LRG_697:g.124703T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.4239T>A	ENSP00000374303.8:p.Thr1413=
ENST00000424120.6:c.4203T>A MANE Select	ENSP00000403465.1:p.Thr1401=
ENST00000503292.6:c.4203T>A	ENSP00000421809.1:p.Thr1401=
ENST00000506643.5:c.4056T>A	ENSP00000422931.2:p.Thr1352=
ENST00000514039.6:c.432T>A	ENSP00000488534.2:p.Thr144=
ENST00000634028.2:c.4056T>A	ENSP00000488669.2:p.Thr1352=
ENST00000650860.2:c.*1700T>A	ENSP00000498775.1:n.*1700T>A
ENST00000674945.1:c.3879T>A	ENSP00000502333.1:p.Thr1293=
ENST00000675768.1:n.1423T>A
ENST00000680586.1:n.4862T>A
ENST00000389652.9:c.3701T>A
ENST00000424120.5:c.4203T>A	ENSP00000403465.1:p.Thr1401=
ENST00000503292.5:c.4203T>A	ENSP00000421809.1:p.Thr1401=
ENST00000506643.4:c.2531T>A
ENST00000634028.1:c.4009T>A	ENSP00000488669.1:n.4009T>A
NM_001080522.2:c.4203T>A , LRG_697t1:c.4203T>A	NP_001073991.2:p.Thr1401=
XM_005248177.1:c.4203T>A	XP_005248234.1:p.Thr1401=
XM_011513869.1:c.4221T>A	XP_011512171.1:p.Thr1407=
XM_011513870.1:c.4221T>A	XP_011512172.1:p.Thr1407=
XM_011513871.1:c.4074T>A	XP_011512173.1:p.Thr1358=
XM_017008482.1:c.4056T>A	XP_016863971.1:p.Thr1352=
NM_001378615.1:c.4203T>A MANE Select	NP_001365544.1:p.Thr1401=
NM_001378617.1:c.4056T>A	NP_001365546.1:p.Thr1352=