Canonical Allele Identifier: CA2154900292

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272744_91272745delinsGA , CM000676.2:g.91272744_91272745delinsGA	GRCh38
NC_000014.8:g.91739088_91739089delinsGA , CM000676.1:g.91739088_91739089delinsGA	GRCh37
NC_000014.7:g.90808841_90808842delinsGA	NCBI36
NG_033118.1:g.150100_150101delinsTC
NG_033118.2:g.150100_150101delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5967_5968delinsTC MANE Select	ENSP00000374507.6:p.Ala1989=
ENST00000331194.8:c.1401_1402delinsTC	ENSP00000330332.8:p.Ala467=
ENST00000389857.10:c.5967_5968delinsTC	ENSP00000374507.6:p.Ala1989=
ENST00000556726.5:c.2195_2196delinsTC
NM_001080414.3:c.5967_5968delinsTC	NP_001073883.2:p.Ala1989=
XM_011536796.1:c.5859_5860delinsTC	XP_011535098.1:p.Ala1953=
XM_011536796.2:c.5859_5860delinsTC	XP_011535098.1:p.Ala1953=
XM_017021336.1:c.3048_3049delinsTC	XP_016876825.1:p.Ala1016=
NM_001080414.4:c.5967_5968delinsTC MANE Select	NP_001073883.2:p.Ala1989=