Canonical Allele Identifier: CA2154902662

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273542T= , CM000676.2:g.91273542T=	GRCh38
NC_000014.8:g.91739886T= , CM000676.1:g.91739886T=	GRCh37
NC_000014.7:g.90809639T=	NCBI36
NG_033118.1:g.149303A=
NG_033118.2:g.149303A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5170A= MANE Select	ENSP00000374507.6:p.Met1724=
ENST00000331194.8:c.742A=	ENSP00000330332.8:p.Met248=
ENST00000334448.5:n.982A=
ENST00000389857.10:c.5170A=	ENSP00000374507.6:p.Met1724=
ENST00000556726.5:c.1398A=
NM_001080414.3:c.5170A=	NP_001073883.2:p.Met1724=
XM_011536796.1:c.5062A=	XP_011535098.1:p.Met1688=
XR_429316.2:n.5445A=
XM_011536796.2:c.5062A=	XP_011535098.1:p.Met1688=
XM_017021336.1:c.2251A=	XP_016876825.1:p.Met751=
XR_429316.4:n.5443A=
NM_001080414.4:c.5170A= MANE Select	NP_001073883.2:p.Met1724=