Canonical Allele Identifier: CA2154899691

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272423_91272425delinsAAC , CM000676.2:g.91272423_91272425delinsAAC	GRCh38
NC_000014.8:g.91738767_91738769delinsAAC , CM000676.1:g.91738767_91738769delinsAAC	GRCh37
NC_000014.7:g.90808520_90808522delinsAAC	NCBI36
NG_033118.1:g.150420_150422delinsGTT
NG_033118.2:g.150420_150422delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*200_*202delinsGTT MANE Select	ENSP00000374507.6:n.*200_*202delinsGTT
ENST00000331194.8:c.*200_*202delinsGTT	ENSP00000330332.8:n.*200_*202delinsGTT
ENST00000389857.10:c.*200_*202delinsGTT	ENSP00000374507.6:n.*200_*202delinsGTT
ENST00000556726.5:c.2515_2517delinsGTT
NM_001080414.3:c.*200_*202delinsGTT	NP_001073883.2:n.*200_*202delinsGTT
XM_011536796.1:c.*200_*202delinsGTT	XP_011535098.1:n.*200_*202delinsGTT
XM_011536796.2:c.*200_*202delinsGTT	XP_011535098.1:n.*200_*202delinsGTT
XM_017021336.1:c.*200_*202delinsGTT	XP_016876825.1:n.*200_*202delinsGTT
NM_001080414.4:c.*200_*202delinsGTT MANE Select	NP_001073883.2:n.*200_*202delinsGTT