Canonical Allele Identifier: CA2154901770

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91306189_91306193delinsCCTTT , CM000676.2:g.91306189_91306193delinsCCTTT	GRCh38
NC_000014.8:g.91772533_91772537delinsCCTTT , CM000676.1:g.91772533_91772537delinsCCTTT	GRCh37
NC_000014.7:g.90842286_90842290delinsCCTTT	NCBI36
NG_033118.1:g.116652_116656delinsAAAGG
NG_033118.2:g.116652_116656delinsAAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3196-267_3196-263delinsAAAGG MANE Select	ENSP00000374507.6:n.3196-267_3196-263delinsAAAGG
ENST00000389857.10:c.3196-267_3196-263delinsAAAGG	ENSP00000374507.6:n.3196-267_3196-263delinsAAAGG
NM_001080414.3:c.3196-267_3196-263delinsAAAGG	NP_001073883.2:n.3196-267_3196-263delinsAAAGG
XM_005267691.3:c.3196-267_3196-263delinsAAAGG	XP_005267748.1:n.3196-267_3196-263delinsAAAGG
XM_011536796.1:c.3088-267_3088-263delinsAAAGG	XP_011535098.1:n.3088-267_3088-263delinsAAAGG
XR_429316.2:n.3324-267_3324-263delinsAAAGG
XR_943459.1:n.3324-267_3324-263delinsAAAGG
XM_005267691.5:c.3196-267_3196-263delinsAAAGG	XP_005267748.1:n.3196-267_3196-263delinsAAAGG
XM_011536796.2:c.3088-267_3088-263delinsAAAGG	XP_011535098.1:n.3088-267_3088-263delinsAAAGG
XM_017021335.2:c.3196-267_3196-263delinsAAAGG	XP_016876824.1:n.3196-267_3196-263delinsAAAGG
XM_017021336.1:c.277-267_277-263delinsAAAGG	XP_016876825.1:n.277-267_277-263delinsAAAGG
XR_429316.4:n.3322-267_3322-263delinsAAAGG
NM_001080414.4:c.3196-267_3196-263delinsAAAGG MANE Select	NP_001073883.2:n.3196-267_3196-263delinsAAAGG