Canonical Allele Identifier: CA390610862

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91273605-C-T
• MyVariant Identifiers: chr14:g.91739949C>T (hg19) ; chr14:g.91273605C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273605C>T , CM000676.2:g.91273605C>T	GRCh38
NC_000014.8:g.91739949C>T , CM000676.1:g.91739949C>T	GRCh37
NC_000014.7:g.90809702C>T	NCBI36
NG_033118.1:g.149240G>A
NG_033118.2:g.149240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5107G>A MANE Select	ENSP00000374507.6:p.Ala1703Thr
ENST00000331194.8:c.679G>A	ENSP00000330332.8:p.Ala227Thr
ENST00000334448.5:n.919G>A
ENST00000389857.10:c.5107G>A	ENSP00000374507.6:p.Ala1703Thr
ENST00000556726.5:c.1335G>A
NM_001080414.3:c.5107G>A	NP_001073883.2:p.Ala1703Thr
XM_011536796.1:c.4999G>A	XP_011535098.1:p.Ala1667Thr
XR_429316.2:n.5382G>A
XM_011536796.2:c.4999G>A	XP_011535098.1:p.Ala1667Thr
XM_017021336.1:c.2188G>A	XP_016876825.1:p.Ala730Thr
XR_429316.4:n.5380G>A
NM_001080414.4:c.5107G>A MANE Select	NP_001073883.2:p.Ala1703Thr