Canonical Allele Identifier: CA2154900269

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272741G= , CM000676.2:g.91272741G=	GRCh38
NC_000014.8:g.91739085G= , CM000676.1:g.91739085G=	GRCh37
NC_000014.7:g.90808838G=	NCBI36
NG_033118.1:g.150104C=
NG_033118.2:g.150104C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5971C= MANE Select	ENSP00000374507.6:p.His1991=
ENST00000331194.8:c.1405C=	ENSP00000330332.8:p.His469=
ENST00000389857.10:c.5971C=	ENSP00000374507.6:p.His1991=
ENST00000556726.5:c.2199C=
NM_001080414.3:c.5971C=	NP_001073883.2:p.His1991=
XM_011536796.1:c.5863C=	XP_011535098.1:p.His1955=
XM_011536796.2:c.5863C=	XP_011535098.1:p.His1955=
XM_017021336.1:c.3052C=	XP_016876825.1:p.His1018=
NM_001080414.4:c.5971C= MANE Select	NP_001073883.2:p.His1991=