Canonical Allele Identifier: CA7309707

Gene: CCDC88C

Linked Data

• ClinVar Variation Id: 2970658
• ClinVar RCV Id: RCV003824360
• dbSNP Id: rs750426113
• ExAC: 14:91779913 C / T
• gnomAD v2: 14-91779913-C-T
• gnomAD v3: 14-91313569-C-T
• gnomAD v4: 14-91313569-C-T
• MyVariant Identifiers: chr14:g.91779913C>T (hg19) ; chr14:g.91313569C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313569C>T , CM000676.2:g.91313569C>T	GRCh38
NC_000014.8:g.91779913C>T , CM000676.1:g.91779913C>T	GRCh37
NC_000014.7:g.90849666C>T	NCBI36
NG_033118.1:g.109276G>A
NG_033118.2:g.109276G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2247G>A MANE Select	ENSP00000374507.6:p.Ala749=
ENST00000389857.10:c.2247G>A	ENSP00000374507.6:p.Ala749=
NM_001080414.3:c.2247G>A	NP_001073883.2:p.Ala749=
XM_005267691.3:c.2247G>A	XP_005267748.1:p.Ala749=
XM_011536796.1:c.2139G>A	XP_011535098.1:p.Ala713=
XR_429316.2:n.2375G>A
XR_943459.1:n.2375G>A
XM_005267691.5:c.2247G>A	XP_005267748.1:p.Ala749=
XM_011536796.2:c.2139G>A	XP_011535098.1:p.Ala713=
XM_017021335.2:c.2247G>A	XP_016876824.1:p.Ala749=
XM_017021337.2:c.2247G>A	XP_016876826.1:p.Ala749=
XR_429316.4:n.2373G>A
NM_001080414.4:c.2247G>A MANE Select	NP_001073883.2:p.Ala749=