Canonical Allele Identifier: CA390610444
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91273458T>A , CM000676.2:g.91273458T>A GRCh38
NC_000014.8:g.91739802T>A , CM000676.1:g.91739802T>A GRCh37
NC_000014.7:g.90809555T>A NCBI36
NG_033118.1:g.149387A>T
NG_033118.2:g.149387A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5254A>T MANE Select ENSP00000374507.6:p.Lys1752Ter
ENST00000331194.8:c.826A>T ENSP00000330332.8:p.Lys276Ter
ENST00000389857.10:c.5254A>T ENSP00000374507.6:p.Lys1752Ter
ENST00000556726.5:c.1482A>T
NM_001080414.3:c.5254A>T NP_001073883.2:p.Lys1752Ter
XM_011536796.1:c.5146A>T XP_011535098.1:p.Lys1716Ter
XM_011536796.2:c.5146A>T XP_011535098.1:p.Lys1716Ter
XM_017021336.1:c.2335A>T XP_016876825.1:p.Lys779Ter
NM_001080414.4:c.5254A>T MANE Select NP_001073883.2:p.Lys1752Ter