Canonical Allele Identifier: CA390607994
Gene: CCDC88C HGNC NCBI

Linked Data

dbSNP Id: rs10142844

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272666C>A , CM000676.2:g.91272666C>A GRCh38
NC_000014.8:g.91739010C>A , CM000676.1:g.91739010C>A GRCh37
NC_000014.7:g.90808763C>A NCBI36
NG_033118.1:g.150179G>T
NG_033118.2:g.150179G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.6046G>T MANE Select ENSP00000374507.6:p.Gly2016Trp
ENST00000331194.8:c.1480G>T ENSP00000330332.8:p.Gly494Trp
ENST00000389857.10:c.6046G>T ENSP00000374507.6:p.Gly2016Trp
ENST00000556726.5:c.2274G>T
NM_001080414.3:c.6046G>T NP_001073883.2:p.Gly2016Trp
XM_011536796.1:c.5938G>T XP_011535098.1:p.Gly1980Trp
XM_011536796.2:c.5938G>T XP_011535098.1:p.Gly1980Trp
XM_017021336.1:c.3127G>T XP_016876825.1:p.Gly1043Trp
NM_001080414.4:c.6046G>T MANE Select NP_001073883.2:p.Gly2016Trp