Canonical Allele Identifier: CA2154888353

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91297215T= , CM000676.2:g.91297215T=	GRCh38
NC_000014.8:g.91763559T= , CM000676.1:g.91763559T=	GRCh37
NC_000014.7:g.90833312T=	NCBI36
NG_033118.1:g.125630A=
NG_033118.2:g.125630A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.3966+90A= MANE Select	ENSP00000374507.6:n.3966+90A=
ENST00000389857.10:c.3966+90A=	ENSP00000374507.6:n.3966+90A=
NM_001080414.3:c.3966+90A=	NP_001073883.2:n.3966+90A=
XM_005267691.3:c.3966+90A=	XP_005267748.1:n.3966+90A=
XM_011536796.1:c.3858+90A=	XP_011535098.1:n.3858+90A=
XR_429316.2:n.4094+90A=
XR_943459.1:n.4094+90A=
XM_005267691.5:c.3966+90A=	XP_005267748.1:n.3966+90A=
XM_011536796.2:c.3858+90A=	XP_011535098.1:n.3858+90A=
XM_017021335.2:c.3966+90A=	XP_016876824.1:n.3966+90A=
XM_017021336.1:c.1047+90A=	XP_016876825.1:n.1047+90A=
XR_429316.4:n.4092+90A=
NM_001080414.4:c.3966+90A= MANE Select	NP_001073883.2:n.3966+90A=