Canonical Allele Identifier: CA2154899652

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272379_91272380delinsAT , CM000676.2:g.91272379_91272380delinsAT	GRCh38
NC_000014.8:g.91738723_91738724delinsAT , CM000676.1:g.91738723_91738724delinsAT	GRCh37
NC_000014.7:g.90808476_90808477delinsAT	NCBI36
NG_033118.1:g.150465_150466delinsAT
NG_033118.2:g.150465_150466delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*245_*246delinsAT MANE Select	ENSP00000374507.6:n.*245_*246delinsAT
ENST00000331194.8:c.*245_*246delinsAT	ENSP00000330332.8:n.*245_*246delinsAT
ENST00000389857.10:c.*245_*246delinsAT	ENSP00000374507.6:n.*245_*246delinsAT
ENST00000556726.5:c.2560_2561delinsAT
NM_001080414.3:c.*245_*246delinsAT	NP_001073883.2:n.*245_*246delinsAT
XM_011536796.1:c.*245_*246delinsAT	XP_011535098.1:n.*245_*246delinsAT
XM_011536796.2:c.*245_*246delinsAT	XP_011535098.1:n.*245_*246delinsAT
XM_017021336.1:c.*245_*246delinsAT	XP_016876825.1:n.*245_*246delinsAT
NM_001080414.4:c.*245_*246delinsAT MANE Select	NP_001073883.2:n.*245_*246delinsAT