Canonical Allele Identifier: CA2154912528

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91337862A= , CM000676.2:g.91337862A=	GRCh38
NC_000014.8:g.91804206A= , CM000676.1:g.91804206A=	GRCh37
NC_000014.7:g.90873959A=	NCBI36
NG_033118.1:g.84983T=
NG_033118.2:g.84983T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.1050+143T= MANE Select	ENSP00000374507.6:n.1050+143T=
ENST00000389857.10:c.1050+143T=	ENSP00000374507.6:n.1050+143T=
NM_001080414.3:c.1050+143T=	NP_001073883.2:n.1050+143T=
XM_005267691.3:c.1050+143T=	XP_005267748.1:n.1050+143T=
XM_011536796.1:c.942+143T=	XP_011535098.1:n.942+143T=
XR_429316.2:n.1178+143T=
XR_943459.1:n.1178+143T=
XM_005267691.5:c.1050+143T=	XP_005267748.1:n.1050+143T=
XM_011536796.2:c.942+143T=	XP_011535098.1:n.942+143T=
XM_017021335.2:c.1050+143T=	XP_016876824.1:n.1050+143T=
XM_017021337.2:c.1050+143T=	XP_016876826.1:n.1050+143T=
XR_429316.4:n.1176+143T=
NM_001080414.4:c.1050+143T= MANE Select	NP_001073883.2:n.1050+143T=