Canonical Allele Identifier: CA2154902227

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273395G= , CM000676.2:g.91273395G=	GRCh38
NC_000014.8:g.91739739G= , CM000676.1:g.91739739G=	GRCh37
NC_000014.7:g.90809492G=	NCBI36
NG_033118.1:g.149450C=
NG_033118.2:g.149450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5317C= MANE Select	ENSP00000374507.6:p.Pro1773=
ENST00000331194.8:c.889C=	ENSP00000330332.8:p.Pro297=
ENST00000389857.10:c.5317C=	ENSP00000374507.6:p.Pro1773=
ENST00000556726.5:c.1545C=
NM_001080414.3:c.5317C=	NP_001073883.2:p.Pro1773=
XM_011536796.1:c.5209C=	XP_011535098.1:p.Pro1737=
XM_011536796.2:c.5209C=	XP_011535098.1:p.Pro1737=
XM_017021336.1:c.2398C=	XP_016876825.1:p.Pro800=
NM_001080414.4:c.5317C= MANE Select	NP_001073883.2:p.Pro1773=