Canonical Allele Identifier: CA2154903192

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273787_91273789delinsCAT , CM000676.2:g.91273787_91273789delinsCAT	GRCh38
NC_000014.8:g.91740131_91740133delinsCAT , CM000676.1:g.91740131_91740133delinsCAT	GRCh37
NC_000014.7:g.90809884_90809886delinsCAT	NCBI36
NG_033118.1:g.149056_149058delinsATG
NG_033118.2:g.149056_149058delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5059-136_5059-134delinsATG MANE Select	ENSP00000374507.6:n.5059-136_5059-134delinsATG
ENST00000331194.8:c.631-136_631-134delinsATG	ENSP00000330332.8:n.631-136_631-134delinsATG
ENST00000334448.5:n.871-136_871-134delinsATG
ENST00000389857.10:c.5059-136_5059-134delinsATG	ENSP00000374507.6:n.5059-136_5059-134delinsATG
ENST00000556726.5:c.1287-136_1287-134delinsATG
NM_001080414.3:c.5059-136_5059-134delinsATG	NP_001073883.2:n.5059-136_5059-134delinsATG
XM_011536796.1:c.4951-136_4951-134delinsATG	XP_011535098.1:n.4951-136_4951-134delinsATG
XR_429316.2:n.5334-136_5334-134delinsATG
XM_011536796.2:c.4951-136_4951-134delinsATG	XP_011535098.1:n.4951-136_4951-134delinsATG
XM_017021336.1:c.2140-136_2140-134delinsATG	XP_016876825.1:n.2140-136_2140-134delinsATG
XR_429316.4:n.5332-136_5332-134delinsATG
NM_001080414.4:c.5059-136_5059-134delinsATG MANE Select	NP_001073883.2:n.5059-136_5059-134delinsATG