Canonical Allele Identifier: CA390608544
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272816C>A , CM000676.2:g.91272816C>A GRCh38
NC_000014.8:g.91739160C>A , CM000676.1:g.91739160C>A GRCh37
NC_000014.7:g.90808913C>A NCBI36
NG_033118.1:g.150029G>T
NG_033118.2:g.150029G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5896G>T MANE Select ENSP00000374507.6:p.Asp1966Tyr
ENST00000331194.8:c.1330G>T ENSP00000330332.8:p.Asp444Tyr
ENST00000389857.10:c.5896G>T ENSP00000374507.6:p.Asp1966Tyr
ENST00000556726.5:c.2124G>T
NM_001080414.3:c.5896G>T NP_001073883.2:p.Asp1966Tyr
XM_011536796.1:c.5788G>T XP_011535098.1:p.Asp1930Tyr
XM_011536796.2:c.5788G>T XP_011535098.1:p.Asp1930Tyr
XM_017021336.1:c.2977G>T XP_016876825.1:p.Asp993Tyr
NM_001080414.4:c.5896G>T MANE Select NP_001073883.2:p.Asp1966Tyr