Canonical Allele Identifier: CA2154900728

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272887T= , CM000676.2:g.91272887T=	GRCh38
NC_000014.8:g.91739231T= , CM000676.1:g.91739231T=	GRCh37
NC_000014.7:g.90808984T=	NCBI36
NG_033118.1:g.149958A=
NG_033118.2:g.149958A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5825A= MANE Select	ENSP00000374507.6:p.Lys1942=
ENST00000331194.8:c.1259A=	ENSP00000330332.8:p.Lys420=
ENST00000389857.10:c.5825A=	ENSP00000374507.6:p.Lys1942=
ENST00000556726.5:c.2053A=
NM_001080414.3:c.5825A=	NP_001073883.2:p.Lys1942=
XM_011536796.1:c.5717A=	XP_011535098.1:p.Lys1906=
XM_011536796.2:c.5717A=	XP_011535098.1:p.Lys1906=
XM_017021336.1:c.2906A=	XP_016876825.1:p.Lys969=
NM_001080414.4:c.5825A= MANE Select	NP_001073883.2:p.Lys1942=