Canonical Allele Identifier: CA2760537920

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15480857_15480858insA , CM000666.2:g.15480857_15480858insA	GRCh38
NC_000004.11:g.15482481_15482482insA , CM000666.1:g.15482481_15482482insA	GRCh37
NC_000004.10:g.15091579_15091580insA	NCBI36
NG_013035.1:g.15993_15994insA , LRG_697:g.15993_15994insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.247+30_247+31insA	ENSP00000374303.8:n.247+30_247+31insA
ENST00000424120.6:c.247+30_247+31insA MANE Select	ENSP00000403465.1:n.247+30_247+31insA
ENST00000503292.6:c.247+30_247+31insA	ENSP00000421809.1:n.247+30_247+31insA
ENST00000506643.5:c.100+30_100+31insA	ENSP00000422931.2:n.100+30_100+31insA
ENST00000511544.6:c.*135+30_*135+31insA	ENSP00000426109.2:n.*135+30_*135+31insA
ENST00000512702.6:c.247+30_247+31insA	ENSP00000422875.2:n.247+30_247+31insA
ENST00000514450.3:c.247+30_247+31insA	ENSP00000502062.1:n.247+30_247+31insA
ENST00000515124.6:c.247+30_247+31insA	ENSP00000424368.1:n.247+30_247+31insA
ENST00000634028.2:c.100+30_100+31insA	ENSP00000488669.2:n.100+30_100+31insA
ENST00000650860.2:c.100+30_100+31insA	ENSP00000498775.1:n.100+30_100+31insA
ENST00000651385.1:c.100+30_100+31insA	ENSP00000499005.1:n.100+30_100+31insA
ENST00000652443.1:c.100+30_100+31insA	ENSP00000502719.1:n.100+30_100+31insA
ENST00000674945.1:c.100+30_100+31insA	ENSP00000502333.1:n.100+30_100+31insA
ENST00000676337.1:c.100+30_100+31insA	ENSP00000501728.1:n.100+30_100+31insA
ENST00000424120.5:c.247+30_247+31insA	ENSP00000403465.1:n.247+30_247+31insA
ENST00000438599.6:c.353+30_353+31insA	ENSP00000401154.2:n.353+30_353+31insA
ENST00000503292.5:c.247+30_247+31insA	ENSP00000421809.1:n.247+30_247+31insA
ENST00000503658.2:c.353+30_353+31insA	ENSP00000426846.1:n.353+30_353+31insA
ENST00000507954.5:c.247+30_247+31insA	ENSP00000427221.1:n.247+30_247+31insA
ENST00000511544.5:c.*135+30_*135+31insA	ENSP00000426109.2:n.*135+30_*135+31insA
ENST00000512702.5:c.247+30_247+31insA	ENSP00000422875.1:n.247+30_247+31insA
ENST00000513811.5:n.427+30_427+31insA
ENST00000514450.2:n.402+30_402+31insA
ENST00000515124.5:c.247+30_247+31insA	ENSP00000424368.1:n.247+30_247+31insA
ENST00000634028.1:c.230+30_230+31insA	ENSP00000488669.1:n.230+30_230+31insA
NM_001080522.2:c.247+30_247+31insA , LRG_697t1:c.247+30_247+31insA	NP_001073991.2:n.247+30_247+31insA
NM_001164720.1:c.247+30_247+31insA	NP_001158192.1:n.247+30_247+31insA
NM_020785.2:c.353+30_353+31insA , LRG_697t2:c.353+30_353+31insA	NP_065836.2:n.353+30_353+31insA
XM_005248177.1:c.247+30_247+31insA	XP_005248234.1:n.247+30_247+31insA
XM_011513869.1:c.247+30_247+31insA	XP_011512171.1:n.247+30_247+31insA
XM_011513870.1:c.247+30_247+31insA	XP_011512172.1:n.247+30_247+31insA
XM_011513871.1:c.100+30_100+31insA	XP_011512173.1:n.100+30_100+31insA
XM_011513872.1:c.247+30_247+31insA	XP_011512174.1:n.247+30_247+31insA
XM_011513873.1:c.247+30_247+31insA	XP_011512175.1:n.247+30_247+31insA
XM_011513874.1:c.247+30_247+31insA	XP_011512176.1:n.247+30_247+31insA
XM_011513872.3:c.247+30_247+31insA	XP_011512174.1:n.247+30_247+31insA
XM_011513874.2:c.247+30_247+31insA	XP_011512176.1:n.247+30_247+31insA
XM_017008482.1:c.100+30_100+31insA	XP_016863971.1:n.100+30_100+31insA
XR_001741296.1:n.447+30_447+31insA
NM_001164720.2:c.247+30_247+31insA	NP_001158192.1:n.247+30_247+31insA
NM_001164720.3:c.247+30_247+31insA	NP_001158192.1:n.247+30_247+31insA
NM_001378615.1:c.247+30_247+31insA MANE Select	NP_001365544.1:n.247+30_247+31insA
NM_001378617.1:c.100+30_100+31insA	NP_001365546.1:n.100+30_100+31insA