Canonical Allele Identifier: CA338306
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 216491
dbSNP Id: rs373960465
gnomAD v2: 4-15565009-G-A
gnomAD v3: 4-15563386-G-A
gnomAD v4: 4-15563386-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15563386G>A , CM000666.2:g.15563386G>A GRCh38
NC_000004.11:g.15565009G>A , CM000666.1:g.15565009G>A GRCh37
NC_000004.10:g.15174107G>A NCBI36
NG_013035.1:g.98521G>A , LRG_697:g.98521G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389652.11:c.3061G>A ENSP00000374303.8:p.Glu1021Lys
ENST00000424120.6:c.3046G>A MANE Select ENSP00000403465.1:p.Glu1016Lys
ENST00000503292.6:c.3046G>A ENSP00000421809.1:p.Glu1016Lys
ENST00000506643.5:c.2899G>A ENSP00000422931.2:p.Glu967Lys
ENST00000634028.2:c.2899G>A ENSP00000488669.2:p.Glu967Lys
ENST00000650860.2:c.*52G>A ENSP00000498775.1:n.*52G>A
ENST00000674945.1:c.2899G>A ENSP00000502333.1:p.Glu967Lys
ENST00000675619.1:n.3857G>A
ENST00000675768.1:n.266G>A
ENST00000676337.1:c.*52G>A ENSP00000501728.1:n.*52G>A
ENST00000680586.1:n.3705G>A
ENST00000389652.9:c.2523G>A
ENST00000424120.5:c.3046G>A ENSP00000403465.1:p.Glu1016Lys
ENST00000503292.5:c.3046G>A ENSP00000421809.1:p.Glu1016Lys
ENST00000506643.4:c.1374G>A
ENST00000634028.1:c.3029G>A ENSP00000488669.1:n.3029G>A
NM_001080522.2:c.3046G>A , LRG_697t1:c.3046G>A NP_001073991.2:p.Glu1016Lys
XM_005248177.1:c.3046G>A XP_005248234.1:p.Glu1016Lys
XM_011513869.1:c.3046G>A XP_011512171.1:p.Glu1016Lys
XM_011513870.1:c.3046G>A XP_011512172.1:p.Glu1016Lys
XM_011513871.1:c.2899G>A XP_011512173.1:p.Glu967Lys
XM_011513872.1:c.*32G>A XP_011512174.1:n.*32G>A
XM_011513872.3:c.*32G>A XP_011512174.1:n.*32G>A
XM_017008482.1:c.2899G>A XP_016863971.1:p.Glu967Lys
XR_001741296.1:n.3291G>A
NM_001378615.1:c.3046G>A MANE Select NP_001365544.1:p.Glu1016Lys
NM_001378617.1:c.2899G>A NP_001365546.1:p.Glu967Lys