Canonical Allele Identifier: CA390610837
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91273593G>A , CM000676.2:g.91273593G>A GRCh38
NC_000014.8:g.91739937G>A , CM000676.1:g.91739937G>A GRCh37
NC_000014.7:g.90809690G>A NCBI36
NG_033118.1:g.149252C>T
NG_033118.2:g.149252C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5119C>T MANE Select ENSP00000374507.6:p.Pro1707Ser
ENST00000331194.8:c.691C>T ENSP00000330332.8:p.Pro231Ser
ENST00000334448.5:n.931C>T
ENST00000389857.10:c.5119C>T ENSP00000374507.6:p.Pro1707Ser
ENST00000556726.5:c.1347C>T
NM_001080414.3:c.5119C>T NP_001073883.2:p.Pro1707Ser
XM_011536796.1:c.5011C>T XP_011535098.1:p.Pro1671Ser
XR_429316.2:n.5394C>T
XM_011536796.2:c.5011C>T XP_011535098.1:p.Pro1671Ser
XM_017021336.1:c.2200C>T XP_016876825.1:p.Pro734Ser
XR_429316.4:n.5392C>T
NM_001080414.4:c.5119C>T MANE Select NP_001073883.2:p.Pro1707Ser