Canonical Allele Identifier: CA390608565

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91272820-C-A
• MyVariant Identifiers: chr14:g.91739164C>A (hg19) ; chr14:g.91272820C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272820C>A , CM000676.2:g.91272820C>A	GRCh38
NC_000014.8:g.91739164C>A , CM000676.1:g.91739164C>A	GRCh37
NC_000014.7:g.90808917C>A	NCBI36
NG_033118.1:g.150025G>T
NG_033118.2:g.150025G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5892G>T MANE Select	ENSP00000374507.6:p.Glu1964Asp
ENST00000331194.8:c.1326G>T	ENSP00000330332.8:p.Glu442Asp
ENST00000389857.10:c.5892G>T	ENSP00000374507.6:p.Glu1964Asp
ENST00000556726.5:c.2120G>T
NM_001080414.3:c.5892G>T	NP_001073883.2:p.Glu1964Asp
XM_011536796.1:c.5784G>T	XP_011535098.1:p.Glu1928Asp
XM_011536796.2:c.5784G>T	XP_011535098.1:p.Glu1928Asp
XM_017021336.1:c.2973G>T	XP_016876825.1:p.Glu991Asp
NM_001080414.4:c.5892G>T MANE Select	NP_001073883.2:p.Glu1964Asp