Canonical Allele Identifier: CA2154909515

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279354T= , CM000676.2:g.91279354T=	GRCh38
NC_000014.8:g.91745698T= , CM000676.1:g.91745698T=	GRCh37
NC_000014.7:g.90815451T=	NCBI36
NG_033118.1:g.143491A=
NG_033118.2:g.143491A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4700-48A= MANE Select	ENSP00000374507.6:n.4700-48A=
ENST00000331194.8:c.272-48A=	ENSP00000330332.8:n.272-48A=
ENST00000334448.5:n.512-48A=
ENST00000389857.10:c.4700-48A=	ENSP00000374507.6:n.4700-48A=
ENST00000556726.5:c.928-48A=
ENST00000557455.1:n.624A=
NM_001080414.3:c.4700-48A=	NP_001073883.2:n.4700-48A=
XM_011536796.1:c.4592-48A=	XP_011535098.1:n.4592-48A=
XR_429316.2:n.4975-48A=
XR_943459.1:n.5535A=
XM_011536796.2:c.4592-48A=	XP_011535098.1:n.4592-48A=
XM_017021335.2:c.*526A=	XP_016876824.1:n.*526A=
XM_017021336.1:c.1781-48A=	XP_016876825.1:n.1781-48A=
XR_429316.4:n.4973-48A=
NM_001080414.4:c.4700-48A= MANE Select	NP_001073883.2:n.4700-48A=