Canonical Allele Identifier: CA609739774

Gene: CCDC122

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.43859494C>T , CM000675.2:g.43859494C>T	GRCh38
NC_000013.10:g.44433630C>T , CM000675.1:g.44433630C>T	GRCh37
NC_000013.9:g.43331630C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444614.8:c.555+178G>A MANE Select	ENSP00000407763.2:n.555+178G>A
ENST00000444614.7:c.555+178G>A	ENSP00000407763.2:n.555+178G>A
ENST00000470137.5:n.484+178G>A
ENST00000476570.2:n.815+178G>A
NM_144974.3:c.555+178G>A	NP_659411.2:n.555+178G>A
XM_011534943.1:c.555+178G>A	XP_011533245.1:n.555+178G>A
XM_011534944.1:c.555+178G>A	XP_011533246.1:n.555+178G>A
XM_011534945.1:c.555+178G>A	XP_011533247.1:n.555+178G>A
NM_001350617.1:c.192+178G>A	NP_001337546.1:n.192+178G>A
NM_001350618.1:c.192+178G>A	NP_001337547.1:n.192+178G>A
NM_144974.4:c.555+178G>A	NP_659411.2:n.555+178G>A
XM_017020397.2:c.555+178G>A	XP_016875886.1:n.555+178G>A
XM_017020398.1:c.555+178G>A	XP_016875887.1:n.555+178G>A
XM_017020399.1:c.555+178G>A	XP_016875888.1:n.555+178G>A
XM_024449322.1:c.192+178G>A	XP_024305090.1:n.192+178G>A
XM_024449323.1:c.192+178G>A	XP_024305091.1:n.192+178G>A
XM_024449324.1:c.192+178G>A	XP_024305092.1:n.192+178G>A
XM_024449325.1:c.192+178G>A	XP_024305093.1:n.192+178G>A
XM_024449326.1:c.192+178G>A	XP_024305094.1:n.192+178G>A
XM_024449327.1:c.192+178G>A	XP_024305095.1:n.192+178G>A
NM_144974.5:c.555+178G>A MANE Select	NP_659411.2:n.555+178G>A
NM_001350617.2:c.192+178G>A	NP_001337546.1:n.192+178G>A
NM_001350618.2:c.192+178G>A	NP_001337547.1:n.192+178G>A