Canonical Allele Identifier: CA1440674685
Gene: CC2D2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15510201G= , CM000666.2:g.15510201G= GRCh38
NC_000004.11:g.15511824G= , CM000666.1:g.15511824G= GRCh37
NC_000004.10:g.15120922G= NCBI36
NG_013035.1:g.45336G= , LRG_697:g.45336G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389652.11:c.501G= ENSP00000374303.8:p.Lys167=
ENST00000424120.6:c.501G= MANE Select ENSP00000403465.1:p.Lys167=
ENST00000503292.6:c.501G= ENSP00000421809.1:p.Lys167=
ENST00000506643.5:c.354G= ENSP00000422931.2:p.Lys118=
ENST00000512702.6:c.501G= ENSP00000422875.2:p.Lys167=
ENST00000514450.3:c.501G= ENSP00000502062.1:p.Lys167=
ENST00000634028.2:c.354G= ENSP00000488669.2:p.Lys118=
ENST00000650860.2:c.354G= ENSP00000498775.1:p.Lys118=
ENST00000651385.1:c.354G= ENSP00000499005.1:p.Lys118=
ENST00000674945.1:c.354G= ENSP00000502333.1:p.Lys118=
ENST00000676337.1:c.354G= ENSP00000501728.1:p.Lys118=
ENST00000424120.5:c.501G= ENSP00000403465.1:p.Lys167=
ENST00000503292.5:c.501G= ENSP00000421809.1:p.Lys167=
ENST00000512702.5:c.501G= ENSP00000422875.1:p.Lys167=
ENST00000513811.5:n.681G=
ENST00000514450.2:n.656G=
ENST00000634028.1:c.484G= ENSP00000488669.1:n.484G=
NM_001080522.2:c.501G= , LRG_697t1:c.501G= NP_001073991.2:p.Lys167=
XM_005248177.1:c.501G= XP_005248234.1:p.Lys167=
XM_011513869.1:c.501G= XP_011512171.1:p.Lys167=
XM_011513870.1:c.501G= XP_011512172.1:p.Lys167=
XM_011513871.1:c.354G= XP_011512173.1:p.Lys118=
XM_011513872.1:c.501G= XP_011512174.1:p.Lys167=
XM_011513873.1:c.501G= XP_011512175.1:p.Lys167=
XM_011513872.3:c.501G= XP_011512174.1:p.Lys167=
XM_017008482.1:c.354G= XP_016863971.1:p.Lys118=
XR_001741296.1:n.701G=
NM_001378615.1:c.501G= MANE Select NP_001365544.1:p.Lys167=
NM_001378617.1:c.354G= NP_001365546.1:p.Lys118=