Canonical Allele Identifier: CA2154910490

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91281494T= , CM000676.2:g.91281494T=	GRCh38
NC_000014.8:g.91747838T= , CM000676.1:g.91747838T=	GRCh37
NC_000014.7:g.90817591T=	NCBI36
NG_033118.1:g.141351A=
NG_033118.2:g.141351A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4662A= MANE Select	ENSP00000374507.6:p.Pro1554=
ENST00000331194.8:c.234A=	ENSP00000330332.8:p.Pro78=
ENST00000334448.5:n.327A=
ENST00000389857.10:c.4662A=	ENSP00000374507.6:p.Pro1554=
ENST00000556726.5:c.890A=
NM_001080414.3:c.4662A=	NP_001073883.2:p.Pro1554=
XM_011536796.1:c.4554A=	XP_011535098.1:p.Pro1518=
XR_429316.2:n.4790A=
XR_943459.1:n.4790A=
XM_011536796.2:c.4554A=	XP_011535098.1:p.Pro1518=
XM_017021335.2:c.4662A=	XP_016876824.1:p.Pro1554=
XM_017021336.1:c.1743A=	XP_016876825.1:p.Pro581=
XR_429316.4:n.4788A=
NM_001080414.4:c.4662A= MANE Select	NP_001073883.2:p.Pro1554=