Canonical Allele Identifier: CA2154888334

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91297190_91297192delinsTTC , CM000676.2:g.91297190_91297192delinsTTC	GRCh38
NC_000014.8:g.91763534_91763536delinsTTC , CM000676.1:g.91763534_91763536delinsTTC	GRCh37
NC_000014.7:g.90833287_90833289delinsTTC	NCBI36
NG_033118.1:g.125653_125655delinsGAA
NG_033118.2:g.125653_125655delinsGAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.3966+113_3966+115delinsGAA MANE Select	ENSP00000374507.6:n.3966+113_3966+115delinsGAA
ENST00000389857.10:c.3966+113_3966+115delinsGAA	ENSP00000374507.6:n.3966+113_3966+115delinsGAA
NM_001080414.3:c.3966+113_3966+115delinsGAA	NP_001073883.2:n.3966+113_3966+115delinsGAA
XM_005267691.3:c.3966+113_3966+115delinsGAA	XP_005267748.1:n.3966+113_3966+115delinsGAA
XM_011536796.1:c.3858+113_3858+115delinsGAA	XP_011535098.1:n.3858+113_3858+115delinsGAA
XR_429316.2:n.4094+113_4094+115delinsGAA
XR_943459.1:n.4094+113_4094+115delinsGAA
XM_005267691.5:c.3966+113_3966+115delinsGAA	XP_005267748.1:n.3966+113_3966+115delinsGAA
XM_011536796.2:c.3858+113_3858+115delinsGAA	XP_011535098.1:n.3858+113_3858+115delinsGAA
XM_017021335.2:c.3966+113_3966+115delinsGAA	XP_016876824.1:n.3966+113_3966+115delinsGAA
XM_017021336.1:c.1047+113_1047+115delinsGAA	XP_016876825.1:n.1047+113_1047+115delinsGAA
XR_429316.4:n.4092+113_4092+115delinsGAA
NM_001080414.4:c.3966+113_3966+115delinsGAA MANE Select	NP_001073883.2:n.3966+113_3966+115delinsGAA