Canonical Allele Identifier: CA2154912591

Gene: CCDC88C

Linked Data

• dbSNP Id: rs1715318734

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91337979A>G , CM000676.2:g.91337979A>G	GRCh38
NC_000014.8:g.91804323A>G , CM000676.1:g.91804323A>G	GRCh37
NC_000014.7:g.90874076A>G	NCBI36
NG_033118.1:g.84866T>C
NG_033118.2:g.84866T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.1050+26T>C MANE Select	ENSP00000374507.6:n.1050+26T>C
ENST00000389857.10:c.1050+26T>C	ENSP00000374507.6:n.1050+26T>C
NM_001080414.3:c.1050+26T>C	NP_001073883.2:n.1050+26T>C
XM_005267691.3:c.1050+26T>C	XP_005267748.1:n.1050+26T>C
XM_011536796.1:c.942+26T>C	XP_011535098.1:n.942+26T>C
XR_429316.2:n.1178+26T>C
XR_943459.1:n.1178+26T>C
XM_005267691.5:c.1050+26T>C	XP_005267748.1:n.1050+26T>C
XM_011536796.2:c.942+26T>C	XP_011535098.1:n.942+26T>C
XM_017021335.2:c.1050+26T>C	XP_016876824.1:n.1050+26T>C
XM_017021337.2:c.1050+26T>C	XP_016876826.1:n.1050+26T>C
XR_429316.4:n.1176+26T>C
NM_001080414.4:c.1050+26T>C MANE Select	NP_001073883.2:n.1050+26T>C