Canonical Allele Identifier: CA1440701461

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15567681T= , CM000666.2:g.15567681T=	GRCh38
NC_000004.11:g.15569304T= , CM000666.1:g.15569304T=	GRCh37
NC_000004.10:g.15178402T=	NCBI36
NG_013035.1:g.102816T= , LRG_697:g.102816T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.3308T=	ENSP00000374303.8:p.Leu1103=
ENST00000424120.6:c.3293T= MANE Select	ENSP00000403465.1:p.Leu1098=
ENST00000503292.6:c.3293T=	ENSP00000421809.1:p.Leu1098=
ENST00000506643.5:c.3146T=	ENSP00000422931.2:p.Leu1049=
ENST00000634028.2:c.3146T=	ENSP00000488669.2:p.Leu1049=
ENST00000650860.2:c.*299T=	ENSP00000498775.1:n.*299T=
ENST00000674945.1:c.3146T=	ENSP00000502333.1:p.Leu1049=
ENST00000675619.1:n.4104T=
ENST00000675768.1:n.513T=
ENST00000676337.1:c.*299T=	ENSP00000501728.1:n.*299T=
ENST00000680586.1:n.3952T=
ENST00000389652.9:c.2770T=
ENST00000424120.5:c.3293T=	ENSP00000403465.1:p.Leu1098=
ENST00000503292.5:c.3293T=	ENSP00000421809.1:p.Leu1098=
ENST00000506643.4:c.1621T=
ENST00000634028.1:c.3276T=	ENSP00000488669.1:n.3276T=
NM_001080522.2:c.3293T= , LRG_697t1:c.3293T=	NP_001073991.2:p.Leu1098=
XM_005248177.1:c.3293T=	XP_005248234.1:p.Leu1098=
XM_011513869.1:c.3293T=	XP_011512171.1:p.Leu1098=
XM_011513870.1:c.3293T=	XP_011512172.1:p.Leu1098=
XM_011513871.1:c.3146T=	XP_011512173.1:p.Leu1049=
XM_017008482.1:c.3146T=	XP_016863971.1:p.Leu1049=
XR_001741296.1:n.3538T=
NM_001378615.1:c.3293T= MANE Select	NP_001365544.1:p.Leu1098=
NM_001378617.1:c.3146T=	NP_001365546.1:p.Leu1049=