Canonical Allele Identifier: CA390610807

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273578G>A , CM000676.2:g.91273578G>A	GRCh38
NC_000014.8:g.91739922G>A , CM000676.1:g.91739922G>A	GRCh37
NC_000014.7:g.90809675G>A	NCBI36
NG_033118.1:g.149267C>T
NG_033118.2:g.149267C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001080414.4:c.5134C>T MANE Select	NP_001073883.2:p.Gln1712Ter
ENST00000389857.11:c.5134C>T MANE Select	ENSP00000374507.6:p.Gln1712Ter
NM_001080414.3:c.5134C>T	NP_001073883.2:p.Gln1712Ter
ENST00000331194.8:c.706C>T	ENSP00000330332.8:p.Gln236Ter
ENST00000334448.5:n.946C>T
ENST00000389857.10:c.5134C>T	ENSP00000374507.6:p.Gln1712Ter
ENST00000556726.5:c.1362C>T
XM_011536796.1:c.5026C>T	XP_011535098.1:p.Gln1676Ter
XM_011536796.2:c.5026C>T	XP_011535098.1:p.Gln1676Ter
XM_017021336.1:c.2215C>T	XP_016876825.1:p.Gln739Ter
XR_429316.2:n.5409C>T
XR_429316.4:n.5407C>T