Canonical Allele Identifier: CA2154910489

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91281493A= , CM000676.2:g.91281493A=	GRCh38
NC_000014.8:g.91747837A= , CM000676.1:g.91747837A=	GRCh37
NC_000014.7:g.90817590A=	NCBI36
NG_033118.1:g.141352T=
NG_033118.2:g.141352T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4663T= MANE Select	ENSP00000374507.6:p.Ser1555=
ENST00000331194.8:c.235T=	ENSP00000330332.8:p.Ser79=
ENST00000334448.5:n.328T=
ENST00000389857.10:c.4663T=	ENSP00000374507.6:p.Ser1555=
ENST00000556726.5:c.891T=
NM_001080414.3:c.4663T=	NP_001073883.2:p.Ser1555=
XM_011536796.1:c.4555T=	XP_011535098.1:p.Ser1519=
XR_429316.2:n.4791T=
XR_943459.1:n.4791T=
XM_011536796.2:c.4555T=	XP_011535098.1:p.Ser1519=
XM_017021335.2:c.4663T=	XP_016876824.1:p.Ser1555=
XM_017021336.1:c.1744T=	XP_016876825.1:p.Ser582=
XR_429316.4:n.4789T=
NM_001080414.4:c.4663T= MANE Select	NP_001073883.2:p.Ser1555=