Canonical Allele Identifier: CA1440702615

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15570338G= , CM000666.2:g.15570338G=	GRCh38
NC_000004.11:g.15571961G= , CM000666.1:g.15571961G=	GRCh37
NC_000004.10:g.15181059G=	NCBI36
NG_013035.1:g.105473G= , LRG_697:g.105473G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.3511-60G=	ENSP00000374303.8:n.3511-60G=
ENST00000424120.6:c.3496-60G= MANE Select	ENSP00000403465.1:n.3496-60G=
ENST00000503292.6:c.3496-60G=	ENSP00000421809.1:n.3496-60G=
ENST00000506643.5:c.3349-60G=	ENSP00000422931.2:n.3349-60G=
ENST00000634028.2:c.3349-60G=	ENSP00000488669.2:n.3349-60G=
ENST00000650860.2:c.*502-60G=	ENSP00000498775.1:n.*502-60G=
ENST00000674945.1:c.3349-60G=	ENSP00000502333.1:n.3349-60G=
ENST00000675619.1:n.4307-60G=
ENST00000675768.1:n.716-60G=
ENST00000676337.1:c.*502-60G=	ENSP00000501728.1:n.*502-60G=
ENST00000680586.1:n.4155-60G=
ENST00000389652.9:c.2973-60G=
ENST00000424120.5:c.3496-60G=	ENSP00000403465.1:n.3496-60G=
ENST00000503292.5:c.3496-60G=	ENSP00000421809.1:n.3496-60G=
ENST00000506643.4:c.1824-60G=
ENST00000634028.1:c.3479-60G=	ENSP00000488669.1:n.3479-60G=
NM_001080522.2:c.3496-60G= , LRG_697t1:c.3496-60G=	NP_001073991.2:n.3496-60G=
XM_005248177.1:c.3496-60G=	XP_005248234.1:n.3496-60G=
XM_011513869.1:c.3496-60G=	XP_011512171.1:n.3496-60G=
XM_011513870.1:c.3496-60G=	XP_011512172.1:n.3496-60G=
XM_011513871.1:c.3349-60G=	XP_011512173.1:n.3349-60G=
XM_017008482.1:c.3349-60G=	XP_016863971.1:n.3349-60G=
XR_001741296.1:n.3741-60G=
NM_001378615.1:c.3496-60G= MANE Select	NP_001365544.1:n.3496-60G=
NM_001378617.1:c.3349-60G=	NP_001365546.1:n.3349-60G=