Canonical Allele Identifier: CA390609961
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91273373C>T , CM000676.2:g.91273373C>T GRCh38
NC_000014.8:g.91739717C>T , CM000676.1:g.91739717C>T GRCh37
NC_000014.7:g.90809470C>T NCBI36
NG_033118.1:g.149472G>A
NG_033118.2:g.149472G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5339G>A MANE Select ENSP00000374507.6:p.Gly1780Asp
ENST00000331194.8:c.911G>A ENSP00000330332.8:p.Gly304Asp
ENST00000389857.10:c.5339G>A ENSP00000374507.6:p.Gly1780Asp
ENST00000556726.5:c.1567G>A
NM_001080414.3:c.5339G>A NP_001073883.2:p.Gly1780Asp
XM_011536796.1:c.5231G>A XP_011535098.1:p.Gly1744Asp
XM_011536796.2:c.5231G>A XP_011535098.1:p.Gly1744Asp
XM_017021336.1:c.2420G>A XP_016876825.1:p.Gly807Asp
NM_001080414.4:c.5339G>A MANE Select NP_001073883.2:p.Gly1780Asp