Canonical Allele Identifier: CA2154901452

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305920C= , CM000676.2:g.91305920C=	GRCh38
NC_000014.8:g.91772264C= , CM000676.1:g.91772264C=	GRCh37
NC_000014.7:g.90842017C=	NCBI36
NG_033118.1:g.116925G=
NG_033118.2:g.116925G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3202G= MANE Select	ENSP00000374507.6:p.Ala1068=
ENST00000389857.10:c.3202G=	ENSP00000374507.6:p.Ala1068=
NM_001080414.3:c.3202G=	NP_001073883.2:p.Ala1068=
XM_005267691.3:c.3202G=	XP_005267748.1:p.Ala1068=
XM_011536796.1:c.3094G=	XP_011535098.1:p.Ala1032=
XR_429316.2:n.3330G=
XR_943459.1:n.3330G=
XM_005267691.5:c.3202G=	XP_005267748.1:p.Ala1068=
XM_011536796.2:c.3094G=	XP_011535098.1:p.Ala1032=
XM_017021335.2:c.3202G=	XP_016876824.1:p.Ala1068=
XM_017021336.1:c.283G=	XP_016876825.1:p.Ala95=
XR_429316.4:n.3328G=
NM_001080414.4:c.3202G= MANE Select	NP_001073883.2:p.Ala1068=