Canonical Allele Identifier: CA2154910486

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91281488C= , CM000676.2:g.91281488C=	GRCh38
NC_000014.8:g.91747832C= , CM000676.1:g.91747832C=	GRCh37
NC_000014.7:g.90817585C=	NCBI36
NG_033118.1:g.141357G=
NG_033118.2:g.141357G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4668G= MANE Select	ENSP00000374507.6:p.Leu1556=
ENST00000331194.8:c.240G=	ENSP00000330332.8:p.Leu80=
ENST00000334448.5:n.333G=
ENST00000389857.10:c.4668G=	ENSP00000374507.6:p.Leu1556=
ENST00000556726.5:c.896G=
NM_001080414.3:c.4668G=	NP_001073883.2:p.Leu1556=
XM_011536796.1:c.4560G=	XP_011535098.1:p.Leu1520=
XR_429316.2:n.4796G=
XR_943459.1:n.4796G=
XM_011536796.2:c.4560G=	XP_011535098.1:p.Leu1520=
XM_017021335.2:c.4668G=	XP_016876824.1:p.Leu1556=
XM_017021336.1:c.1749G=	XP_016876825.1:p.Leu583=
XR_429316.4:n.4794G=
NM_001080414.4:c.4668G= MANE Select	NP_001073883.2:p.Leu1556=