Canonical Allele Identifier: CA356412901
Gene: CC2D2A HGNC NCBI

Linked Data

gnomAD v4: 4-15559235-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15559235T>A , CM000666.2:g.15559235T>A GRCh38
NC_000004.11:g.15560858T>A , CM000666.1:g.15560858T>A GRCh37
NC_000004.10:g.15169956T>A NCBI36
NG_013035.1:g.94370T>A , LRG_697:g.94370T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389652.11:c.2900T>A ENSP00000374303.8:p.Ile967Lys
ENST00000424120.6:c.2900T>A MANE Select ENSP00000403465.1:p.Ile967Lys
ENST00000503292.6:c.2900T>A ENSP00000421809.1:p.Ile967Lys
ENST00000506643.5:c.2753T>A ENSP00000422931.2:p.Ile918Lys
ENST00000634028.2:c.2753T>A ENSP00000488669.2:p.Ile918Lys
ENST00000650860.2:c.2753T>A ENSP00000498775.1:p.Ile918Lys
ENST00000674945.1:c.2753T>A ENSP00000502333.1:p.Ile918Lys
ENST00000675619.1:n.979T>A
ENST00000675768.1:n.120T>A
ENST00000676337.1:c.2753T>A ENSP00000501728.1:p.Ile918Lys
ENST00000680586.1:n.827T>A
ENST00000389652.9:c.2362T>A
ENST00000424120.5:c.2900T>A ENSP00000403465.1:p.Ile967Lys
ENST00000503292.5:c.2900T>A ENSP00000421809.1:p.Ile967Lys
ENST00000506643.4:c.1228T>A
ENST00000634028.1:c.2883T>A ENSP00000488669.1:n.2883T>A
NM_001080522.2:c.2900T>A , LRG_697t1:c.2900T>A NP_001073991.2:p.Ile967Lys
XM_005248177.1:c.2900T>A XP_005248234.1:p.Ile967Lys
XM_011513869.1:c.2900T>A XP_011512171.1:p.Ile967Lys
XM_011513870.1:c.2900T>A XP_011512172.1:p.Ile967Lys
XM_011513871.1:c.2753T>A XP_011512173.1:p.Ile918Lys
XM_011513872.1:c.2900T>A XP_011512174.1:p.Ile967Lys
XM_011513873.1:c.2900T>A XP_011512175.1:p.Ile967Lys
XM_011513872.3:c.2900T>A XP_011512174.1:p.Ile967Lys
XM_017008482.1:c.2753T>A XP_016863971.1:p.Ile918Lys
XR_001741296.1:n.3100T>A
NM_001378615.1:c.2900T>A MANE Select NP_001365544.1:p.Ile967Lys
NM_001378617.1:c.2753T>A NP_001365546.1:p.Ile918Lys