Canonical Allele Identifier: CA1440701462

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15567683G= , CM000666.2:g.15567683G=	GRCh38
NC_000004.11:g.15569306G= , CM000666.1:g.15569306G=	GRCh37
NC_000004.10:g.15178404G=	NCBI36
NG_013035.1:g.102818G= , LRG_697:g.102818G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.3310G=	ENSP00000374303.8:p.Val1104=
ENST00000424120.6:c.3295G= MANE Select	ENSP00000403465.1:p.Val1099=
ENST00000503292.6:c.3295G=	ENSP00000421809.1:p.Val1099=
ENST00000506643.5:c.3148G=	ENSP00000422931.2:p.Val1050=
ENST00000634028.2:c.3148G=	ENSP00000488669.2:p.Val1050=
ENST00000650860.2:c.*301G=	ENSP00000498775.1:n.*301G=
ENST00000674945.1:c.3148G=	ENSP00000502333.1:p.Val1050=
ENST00000675619.1:n.4106G=
ENST00000675768.1:n.515G=
ENST00000676337.1:c.*301G=	ENSP00000501728.1:n.*301G=
ENST00000680586.1:n.3954G=
ENST00000389652.9:c.2772G=
ENST00000424120.5:c.3295G=	ENSP00000403465.1:p.Val1099=
ENST00000503292.5:c.3295G=	ENSP00000421809.1:p.Val1099=
ENST00000506643.4:c.1623G=
ENST00000634028.1:c.3278G=	ENSP00000488669.1:n.3278G=
NM_001080522.2:c.3295G= , LRG_697t1:c.3295G=	NP_001073991.2:p.Val1099=
XM_005248177.1:c.3295G=	XP_005248234.1:p.Val1099=
XM_011513869.1:c.3295G=	XP_011512171.1:p.Val1099=
XM_011513870.1:c.3295G=	XP_011512172.1:p.Val1099=
XM_011513871.1:c.3148G=	XP_011512173.1:p.Val1050=
XM_017008482.1:c.3148G=	XP_016863971.1:p.Val1050=
XR_001741296.1:n.3540G=
NM_001378615.1:c.3295G= MANE Select	NP_001365544.1:p.Val1099=
NM_001378617.1:c.3148G=	NP_001365546.1:p.Val1050=