Canonical Allele Identifier: CA2154901795

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91306210C= , CM000676.2:g.91306210C=	GRCh38
NC_000014.8:g.91772554C= , CM000676.1:g.91772554C=	GRCh37
NC_000014.7:g.90842307C=	NCBI36
NG_033118.1:g.116635G=
NG_033118.2:g.116635G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3196-284G= MANE Select	ENSP00000374507.6:n.3196-284G=
ENST00000389857.10:c.3196-284G=	ENSP00000374507.6:n.3196-284G=
NM_001080414.3:c.3196-284G=	NP_001073883.2:n.3196-284G=
XM_005267691.3:c.3196-284G=	XP_005267748.1:n.3196-284G=
XM_011536796.1:c.3088-284G=	XP_011535098.1:n.3088-284G=
XR_429316.2:n.3324-284G=
XR_943459.1:n.3324-284G=
XM_005267691.5:c.3196-284G=	XP_005267748.1:n.3196-284G=
XM_011536796.2:c.3088-284G=	XP_011535098.1:n.3088-284G=
XM_017021335.2:c.3196-284G=	XP_016876824.1:n.3196-284G=
XM_017021336.1:c.277-284G=	XP_016876825.1:n.277-284G=
XR_429316.4:n.3322-284G=
NM_001080414.4:c.3196-284G= MANE Select	NP_001073883.2:n.3196-284G=