Canonical Allele Identifier: CA2154902415

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273456C= , CM000676.2:g.91273456C=	GRCh38
NC_000014.8:g.91739800C= , CM000676.1:g.91739800C=	GRCh37
NC_000014.7:g.90809553C=	NCBI36
NG_033118.1:g.149389G=
NG_033118.2:g.149389G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5256G= MANE Select	ENSP00000374507.6:p.Lys1752=
ENST00000331194.8:c.828G=	ENSP00000330332.8:p.Lys276=
ENST00000389857.10:c.5256G=	ENSP00000374507.6:p.Lys1752=
ENST00000556726.5:c.1484G=
NM_001080414.3:c.5256G=	NP_001073883.2:p.Lys1752=
XM_011536796.1:c.5148G=	XP_011535098.1:p.Lys1716=
XM_011536796.2:c.5148G=	XP_011535098.1:p.Lys1716=
XM_017021336.1:c.2337G=	XP_016876825.1:p.Lys779=
NM_001080414.4:c.5256G= MANE Select	NP_001073883.2:p.Lys1752=