Canonical Allele Identifier: CA1440701493
Gene: CC2D2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15567755A= , CM000666.2:g.15567755A= GRCh38
NC_000004.11:g.15569378A= , CM000666.1:g.15569378A= GRCh37
NC_000004.10:g.15178476A= NCBI36
NG_013035.1:g.102890A= , LRG_697:g.102890A=

Transcript Alleles

HGVS Amino-acid change
ENST00000389652.11:c.3382A= ENSP00000374303.8:p.Ser1128=
ENST00000424120.6:c.3367A= MANE Select ENSP00000403465.1:p.Ser1123=
ENST00000503292.6:c.3367A= ENSP00000421809.1:p.Ser1123=
ENST00000506643.5:c.3220A= ENSP00000422931.2:p.Ser1074=
ENST00000634028.2:c.3220A= ENSP00000488669.2:p.Ser1074=
ENST00000650860.2:c.*373A= ENSP00000498775.1:n.*373A=
ENST00000674945.1:c.3220A= ENSP00000502333.1:p.Ser1074=
ENST00000675619.1:n.4178A=
ENST00000675768.1:n.587A=
ENST00000676337.1:c.*373A= ENSP00000501728.1:n.*373A=
ENST00000680586.1:n.4026A=
ENST00000389652.9:c.2844A=
ENST00000424120.5:c.3367A= ENSP00000403465.1:p.Ser1123=
ENST00000503292.5:c.3367A= ENSP00000421809.1:p.Ser1123=
ENST00000506643.4:c.1695A=
ENST00000634028.1:c.3350A= ENSP00000488669.1:n.3350A=
NM_001080522.2:c.3367A= , LRG_697t1:c.3367A= NP_001073991.2:p.Ser1123=
XM_005248177.1:c.3367A= XP_005248234.1:p.Ser1123=
XM_011513869.1:c.3367A= XP_011512171.1:p.Ser1123=
XM_011513870.1:c.3367A= XP_011512172.1:p.Ser1123=
XM_011513871.1:c.3220A= XP_011512173.1:p.Ser1074=
XM_017008482.1:c.3220A= XP_016863971.1:p.Ser1074=
XR_001741296.1:n.3612A=
NM_001378615.1:c.3367A= MANE Select NP_001365544.1:p.Ser1123=
NM_001378617.1:c.3220A= NP_001365546.1:p.Ser1074=