Canonical Allele Identifier: CA2154902632

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273532T= , CM000676.2:g.91273532T=	GRCh38
NC_000014.8:g.91739876T= , CM000676.1:g.91739876T=	GRCh37
NC_000014.7:g.90809629T=	NCBI36
NG_033118.1:g.149313A=
NG_033118.2:g.149313A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.5180A= MANE Select	ENSP00000374507.6:p.Asn1727=
ENST00000331194.8:c.752A=	ENSP00000330332.8:p.Asn251=
ENST00000334448.5:n.992A=
ENST00000389857.10:c.5180A=	ENSP00000374507.6:p.Asn1727=
ENST00000556726.5:c.1408A=
NM_001080414.3:c.5180A=	NP_001073883.2:p.Asn1727=
XM_011536796.1:c.5072A=	XP_011535098.1:p.Asn1691=
XR_429316.2:n.5455A=
XM_011536796.2:c.5072A=	XP_011535098.1:p.Asn1691=
XM_017021336.1:c.2261A=	XP_016876825.1:p.Asn754=
XR_429316.4:n.5453A=
NM_001080414.4:c.5180A= MANE Select	NP_001073883.2:p.Asn1727=