Canonical Allele Identifier: CA1440688366

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15540896_15540899delinsTCAA , CM000666.2:g.15540896_15540899delinsTCAA	GRCh38
NC_000004.11:g.15542519_15542522delinsTCAA , CM000666.1:g.15542519_15542522delinsTCAA	GRCh37
NC_000004.10:g.15151617_15151620delinsTCAA	NCBI36
NG_013035.1:g.76031_76034delinsTCAA , LRG_697:g.76031_76034delinsTCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000389652.11:c.2063_2066delinsTCAA	ENSP00000374303.8:p.Phe688=
ENST00000424120.6:c.2063_2066delinsTCAA MANE Select	ENSP00000403465.1:p.Phe688=
ENST00000503292.6:c.2063_2066delinsTCAA	ENSP00000421809.1:p.Phe688=
ENST00000506643.5:c.1916_1919delinsTCAA	ENSP00000422931.2:p.Phe639=
ENST00000634028.2:c.1916_1919delinsTCAA	ENSP00000488669.2:p.Phe639=
ENST00000650860.2:c.1916_1919delinsTCAA	ENSP00000498775.1:p.Phe639=
ENST00000674945.1:c.1916_1919delinsTCAA	ENSP00000502333.1:p.Phe639=
ENST00000675619.1:n.142_145delinsTCAA
ENST00000676337.1:c.1916_1919delinsTCAA	ENSP00000501728.1:p.Phe639=
ENST00000389652.9:c.1525_1528delinsTCAA
ENST00000424120.5:c.2063_2066delinsTCAA	ENSP00000403465.1:p.Phe688=
ENST00000503292.5:c.2063_2066delinsTCAA	ENSP00000421809.1:p.Phe688=
ENST00000506643.4:c.391_394delinsTCAA
ENST00000513811.5:n.2243_2246delinsTCAA
ENST00000634028.1:c.2046_2049delinsTCAA	ENSP00000488669.1:n.2046_2049delinsTCAA
NM_001080522.2:c.2063_2066delinsTCAA , LRG_697t1:c.2063_2066delinsTCAA	NP_001073991.2:p.Phe688=
XM_005248177.1:c.2063_2066delinsTCAA	XP_005248234.1:p.Phe688=
XM_011513869.1:c.2063_2066delinsTCAA	XP_011512171.1:p.Phe688=
XM_011513870.1:c.2063_2066delinsTCAA	XP_011512172.1:p.Phe688=
XM_011513871.1:c.1916_1919delinsTCAA	XP_011512173.1:p.Phe639=
XM_011513872.1:c.2063_2066delinsTCAA	XP_011512174.1:p.Phe688=
XM_011513873.1:c.2063_2066delinsTCAA	XP_011512175.1:p.Phe688=
XM_011513872.3:c.2063_2066delinsTCAA	XP_011512174.1:p.Phe688=
XM_017008482.1:c.1916_1919delinsTCAA	XP_016863971.1:p.Phe639=
XR_001741296.1:n.2263_2266delinsTCAA
NM_001378615.1:c.2063_2066delinsTCAA MANE Select	NP_001365544.1:p.Phe688=
NM_001378617.1:c.1916_1919delinsTCAA	NP_001365546.1:p.Phe639=