Canonical Allele Identifier: CA2154901656

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91306090_91306093delinsTCAG , CM000676.2:g.91306090_91306093delinsTCAG	GRCh38
NC_000014.8:g.91772434_91772437delinsTCAG , CM000676.1:g.91772434_91772437delinsTCAG	GRCh37
NC_000014.7:g.90842187_90842190delinsTCAG	NCBI36
NG_033118.1:g.116752_116755delinsCTGA
NG_033118.2:g.116752_116755delinsCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3196-167_3196-164delinsCTGA MANE Select	ENSP00000374507.6:n.3196-167_3196-164delinsCTGA
ENST00000389857.10:c.3196-167_3196-164delinsCTGA	ENSP00000374507.6:n.3196-167_3196-164delinsCTGA
NM_001080414.3:c.3196-167_3196-164delinsCTGA	NP_001073883.2:n.3196-167_3196-164delinsCTGA
XM_005267691.3:c.3196-167_3196-164delinsCTGA	XP_005267748.1:n.3196-167_3196-164delinsCTGA
XM_011536796.1:c.3088-167_3088-164delinsCTGA	XP_011535098.1:n.3088-167_3088-164delinsCTGA
XR_429316.2:n.3324-167_3324-164delinsCTGA
XR_943459.1:n.3324-167_3324-164delinsCTGA
XM_005267691.5:c.3196-167_3196-164delinsCTGA	XP_005267748.1:n.3196-167_3196-164delinsCTGA
XM_011536796.2:c.3088-167_3088-164delinsCTGA	XP_011535098.1:n.3088-167_3088-164delinsCTGA
XM_017021335.2:c.3196-167_3196-164delinsCTGA	XP_016876824.1:n.3196-167_3196-164delinsCTGA
XM_017021336.1:c.277-167_277-164delinsCTGA	XP_016876825.1:n.277-167_277-164delinsCTGA
XR_429316.4:n.3322-167_3322-164delinsCTGA
NM_001080414.4:c.3196-167_3196-164delinsCTGA MANE Select	NP_001073883.2:n.3196-167_3196-164delinsCTGA