Canonical Allele Identifier: CA390608517
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272812C>G , CM000676.2:g.91272812C>G GRCh38
NC_000014.8:g.91739156C>G , CM000676.1:g.91739156C>G GRCh37
NC_000014.7:g.90808909C>G NCBI36
NG_033118.1:g.150033G>C
NG_033118.2:g.150033G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5900G>C MANE Select ENSP00000374507.6:p.Gly1967Ala
ENST00000331194.8:c.1334G>C ENSP00000330332.8:p.Gly445Ala
ENST00000389857.10:c.5900G>C ENSP00000374507.6:p.Gly1967Ala
ENST00000556726.5:c.2128G>C
NM_001080414.3:c.5900G>C NP_001073883.2:p.Gly1967Ala
XM_011536796.1:c.5792G>C XP_011535098.1:p.Gly1931Ala
XM_011536796.2:c.5792G>C XP_011535098.1:p.Gly1931Ala
XM_017021336.1:c.2981G>C XP_016876825.1:p.Gly994Ala
NM_001080414.4:c.5900G>C MANE Select NP_001073883.2:p.Gly1967Ala