Canonical Allele Identifier: CA2154903002

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273693G= , CM000676.2:g.91273693G=	GRCh38
NC_000014.8:g.91740037G= , CM000676.1:g.91740037G=	GRCh37
NC_000014.7:g.90809790G=	NCBI36
NG_033118.1:g.149152C=
NG_033118.2:g.149152C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5059-40C= MANE Select	ENSP00000374507.6:n.5059-40C=
ENST00000331194.8:c.631-40C=	ENSP00000330332.8:n.631-40C=
ENST00000334448.5:n.871-40C=
ENST00000389857.10:c.5059-40C=	ENSP00000374507.6:n.5059-40C=
ENST00000556726.5:c.1287-40C=
NM_001080414.3:c.5059-40C=	NP_001073883.2:n.5059-40C=
XM_011536796.1:c.4951-40C=	XP_011535098.1:n.4951-40C=
XR_429316.2:n.5334-40C=
XM_011536796.2:c.4951-40C=	XP_011535098.1:n.4951-40C=
XM_017021336.1:c.2140-40C=	XP_016876825.1:n.2140-40C=
XR_429316.4:n.5332-40C=
NM_001080414.4:c.5059-40C= MANE Select	NP_001073883.2:n.5059-40C=