Canonical Allele Identifier: CA390610219

Gene: CCDC88C

Linked Data

• dbSNP Id: rs1483683666
• gnomAD v2: 14-91739762-C-T
• gnomAD v4: 14-91273418-C-T
• MyVariant Identifiers: chr14:g.91739762C>T (hg19) ; chr14:g.91273418C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273418C>T , CM000676.2:g.91273418C>T	GRCh38
NC_000014.8:g.91739762C>T , CM000676.1:g.91739762C>T	GRCh37
NC_000014.7:g.90809515C>T	NCBI36
NG_033118.1:g.149427G>A
NG_033118.2:g.149427G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5294G>A MANE Select	ENSP00000374507.6:p.Ser1765Asn
ENST00000331194.8:c.866G>A	ENSP00000330332.8:p.Ser289Asn
ENST00000389857.10:c.5294G>A	ENSP00000374507.6:p.Ser1765Asn
ENST00000556726.5:c.1522G>A
NM_001080414.3:c.5294G>A	NP_001073883.2:p.Ser1765Asn
XM_011536796.1:c.5186G>A	XP_011535098.1:p.Ser1729Asn
XM_011536796.2:c.5186G>A	XP_011535098.1:p.Ser1729Asn
XM_017021336.1:c.2375G>A	XP_016876825.1:p.Ser792Asn
NM_001080414.4:c.5294G>A MANE Select	NP_001073883.2:p.Ser1765Asn