Canonical Allele Identifier: CA2154902790
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91273626G= , CM000676.2:g.91273626G= GRCh38
NC_000014.8:g.91739970G= , CM000676.1:g.91739970G= GRCh37
NC_000014.7:g.90809723G= NCBI36
NG_033118.1:g.149219C=
NG_033118.2:g.149219C=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.5086C= MANE Select ENSP00000374507.6:p.Leu1696=
ENST00000331194.8:c.658C= ENSP00000330332.8:p.Leu220=
ENST00000334448.5:n.898C=
ENST00000389857.10:c.5086C= ENSP00000374507.6:p.Leu1696=
ENST00000556726.5:c.1314C=
NM_001080414.3:c.5086C= NP_001073883.2:p.Leu1696=
XM_011536796.1:c.4978C= XP_011535098.1:p.Leu1660=
XR_429316.2:n.5361C=
XM_011536796.2:c.4978C= XP_011535098.1:p.Leu1660=
XM_017021336.1:c.2167C= XP_016876825.1:p.Leu723=
XR_429316.4:n.5359C=
NM_001080414.4:c.5086C= MANE Select NP_001073883.2:p.Leu1696=