Canonical Allele Identifier: CA7308864
Gene: CCDC88C HGNC NCBI

Linked Data

dbSNP Id: rs752668368

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91279303G>C , CM000676.2:g.91279303G>C GRCh38
NC_000014.8:g.91745647G>C , CM000676.1:g.91745647G>C GRCh37
NC_000014.7:g.90815400G>C NCBI36
NG_033118.1:g.143542C>G
NG_033118.2:g.143542C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.4703C>G MANE Select ENSP00000374507.6:p.Ser1568Trp
ENST00000331194.8:c.275C>G ENSP00000330332.8:p.Ser92Trp
ENST00000334448.5:n.515C>G
ENST00000389857.10:c.4703C>G ENSP00000374507.6:p.Ser1568Trp
ENST00000556726.5:c.931C>G
ENST00000557455.1:n.675C>G
NM_001080414.3:c.4703C>G NP_001073883.2:p.Ser1568Trp
XM_011536796.1:c.4595C>G XP_011535098.1:p.Ser1532Trp
XR_429316.2:n.4978C>G
XM_011536796.2:c.4595C>G XP_011535098.1:p.Ser1532Trp
XM_017021336.1:c.1784C>G XP_016876825.1:p.Ser595Trp
XR_429316.4:n.4976C>G
NM_001080414.4:c.4703C>G MANE Select NP_001073883.2:p.Ser1568Trp