Canonical Allele Identifier: CA2154899901

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272615C= , CM000676.2:g.91272615C=	GRCh38
NC_000014.8:g.91738959C= , CM000676.1:g.91738959C=	GRCh37
NC_000014.7:g.90808712C=	NCBI36
NG_033118.1:g.150230G=
NG_033118.2:g.150230G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*10G= MANE Select	ENSP00000374507.6:n.*10G=
ENST00000331194.8:c.*10G=	ENSP00000330332.8:n.*10G=
ENST00000389857.10:c.*10G=	ENSP00000374507.6:n.*10G=
ENST00000556726.5:c.2325G=
NM_001080414.3:c.*10G=	NP_001073883.2:n.*10G=
XM_011536796.1:c.*10G=	XP_011535098.1:n.*10G=
XM_011536796.2:c.*10G=	XP_011535098.1:n.*10G=
XM_017021336.1:c.*10G=	XP_016876825.1:n.*10G=
NM_001080414.4:c.*10G= MANE Select	NP_001073883.2:n.*10G=