Canonical Allele Identifier: CA2154901517

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305965T= , CM000676.2:g.91305965T=	GRCh38
NC_000014.8:g.91772309T= , CM000676.1:g.91772309T=	GRCh37
NC_000014.7:g.90842062T=	NCBI36
NG_033118.1:g.116880A=
NG_033118.2:g.116880A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3196-39A= MANE Select	ENSP00000374507.6:n.3196-39A=
ENST00000389857.10:c.3196-39A=	ENSP00000374507.6:n.3196-39A=
NM_001080414.3:c.3196-39A=	NP_001073883.2:n.3196-39A=
XM_005267691.3:c.3196-39A=	XP_005267748.1:n.3196-39A=
XM_011536796.1:c.3088-39A=	XP_011535098.1:n.3088-39A=
XR_429316.2:n.3324-39A=
XR_943459.1:n.3324-39A=
XM_005267691.5:c.3196-39A=	XP_005267748.1:n.3196-39A=
XM_011536796.2:c.3088-39A=	XP_011535098.1:n.3088-39A=
XM_017021335.2:c.3196-39A=	XP_016876824.1:n.3196-39A=
XM_017021336.1:c.277-39A=	XP_016876825.1:n.277-39A=
XR_429316.4:n.3322-39A=
NM_001080414.4:c.3196-39A= MANE Select	NP_001073883.2:n.3196-39A=