Canonical Allele Identifier: CA2154902729

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273584C= , CM000676.2:g.91273584C=	GRCh38
NC_000014.8:g.91739928C= , CM000676.1:g.91739928C=	GRCh37
NC_000014.7:g.90809681C=	NCBI36
NG_033118.1:g.149261G=
NG_033118.2:g.149261G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5128G= MANE Select	ENSP00000374507.6:p.Gly1710=
ENST00000331194.8:c.700G=	ENSP00000330332.8:p.Gly234=
ENST00000334448.5:n.940G=
ENST00000389857.10:c.5128G=	ENSP00000374507.6:p.Gly1710=
ENST00000556726.5:c.1356G=
NM_001080414.3:c.5128G=	NP_001073883.2:p.Gly1710=
XM_011536796.1:c.5020G=	XP_011535098.1:p.Gly1674=
XR_429316.2:n.5403G=
XM_011536796.2:c.5020G=	XP_011535098.1:p.Gly1674=
XM_017021336.1:c.2209G=	XP_016876825.1:p.Gly737=
XR_429316.4:n.5401G=
NM_001080414.4:c.5128G= MANE Select	NP_001073883.2:p.Gly1710=