Canonical Allele Identifier: CA2154901242

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305758C= , CM000676.2:g.91305758C=	GRCh38
NC_000014.8:g.91772102C= , CM000676.1:g.91772102C=	GRCh37
NC_000014.7:g.90841855C=	NCBI36
NG_033118.1:g.117087G=
NG_033118.2:g.117087G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3357+7G= MANE Select	ENSP00000374507.6:n.3357+7G=
ENST00000389857.10:c.3357+7G=	ENSP00000374507.6:n.3357+7G=
NM_001080414.3:c.3357+7G=	NP_001073883.2:n.3357+7G=
XM_005267691.3:c.3357+7G=	XP_005267748.1:n.3357+7G=
XM_011536796.1:c.3249+7G=	XP_011535098.1:n.3249+7G=
XR_429316.2:n.3485+7G=
XR_943459.1:n.3485+7G=
XM_005267691.5:c.3357+7G=	XP_005267748.1:n.3357+7G=
XM_011536796.2:c.3249+7G=	XP_011535098.1:n.3249+7G=
XM_017021335.2:c.3357+7G=	XP_016876824.1:n.3357+7G=
XM_017021336.1:c.438+7G=	XP_016876825.1:n.438+7G=
XR_429316.4:n.3483+7G=
NM_001080414.4:c.3357+7G= MANE Select	NP_001073883.2:n.3357+7G=