Canonical Allele Identifier: CA356418527

Gene: CC2D2A

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15567678T>C , CM000666.2:g.15567678T>C	GRCh38
NC_000004.11:g.15569301T>C , CM000666.1:g.15569301T>C	GRCh37
NC_000004.10:g.15178399T>C	NCBI36
NG_013035.1:g.102813T>C , LRG_697:g.102813T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.3305T>C	ENSP00000374303.8:p.Val1102Ala
ENST00000424120.6:c.3290T>C MANE Select	ENSP00000403465.1:p.Val1097Ala
ENST00000503292.6:c.3290T>C	ENSP00000421809.1:p.Val1097Ala
ENST00000506643.5:c.3143T>C	ENSP00000422931.2:p.Val1048Ala
ENST00000634028.2:c.3143T>C	ENSP00000488669.2:p.Val1048Ala
ENST00000650860.2:c.*296T>C	ENSP00000498775.1:n.*296T>C
ENST00000674945.1:c.3143T>C	ENSP00000502333.1:p.Val1048Ala
ENST00000675619.1:n.4101T>C
ENST00000675768.1:n.510T>C
ENST00000676337.1:c.*296T>C	ENSP00000501728.1:n.*296T>C
ENST00000680586.1:n.3949T>C
ENST00000389652.9:c.2767T>C
ENST00000424120.5:c.3290T>C	ENSP00000403465.1:p.Val1097Ala
ENST00000503292.5:c.3290T>C	ENSP00000421809.1:p.Val1097Ala
ENST00000506643.4:c.1618T>C
ENST00000634028.1:c.3273T>C	ENSP00000488669.1:n.3273T>C
NM_001080522.2:c.3290T>C , LRG_697t1:c.3290T>C	NP_001073991.2:p.Val1097Ala
XM_005248177.1:c.3290T>C	XP_005248234.1:p.Val1097Ala
XM_011513869.1:c.3290T>C	XP_011512171.1:p.Val1097Ala
XM_011513870.1:c.3290T>C	XP_011512172.1:p.Val1097Ala
XM_011513871.1:c.3143T>C	XP_011512173.1:p.Val1048Ala
XM_017008482.1:c.3143T>C	XP_016863971.1:p.Val1048Ala
XR_001741296.1:n.3535T>C
NM_001378615.1:c.3290T>C MANE Select	NP_001365544.1:p.Val1097Ala
NM_001378617.1:c.3143T>C	NP_001365546.1:p.Val1048Ala