Canonical Allele Identifier: CA390613283

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91281492-G-T
• MyVariant Identifiers: chr14:g.91747836G>T (hg19) ; chr14:g.91281492G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91281492G>T , CM000676.2:g.91281492G>T	GRCh38
NC_000014.8:g.91747836G>T , CM000676.1:g.91747836G>T	GRCh37
NC_000014.7:g.90817589G>T	NCBI36
NG_033118.1:g.141353C>A
NG_033118.2:g.141353C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4664C>A MANE Select	ENSP00000374507.6:p.Ser1555Tyr
ENST00000331194.8:c.236C>A	ENSP00000330332.8:p.Ser79Tyr
ENST00000334448.5:n.329C>A
ENST00000389857.10:c.4664C>A	ENSP00000374507.6:p.Ser1555Tyr
ENST00000556726.5:c.892C>A
NM_001080414.3:c.4664C>A	NP_001073883.2:p.Ser1555Tyr
XM_011536796.1:c.4556C>A	XP_011535098.1:p.Ser1519Tyr
XR_429316.2:n.4792C>A
XR_943459.1:n.4792C>A
XM_011536796.2:c.4556C>A	XP_011535098.1:p.Ser1519Tyr
XM_017021335.2:c.4664C>A	XP_016876824.1:p.Ser1555Tyr
XM_017021336.1:c.1745C>A	XP_016876825.1:p.Ser582Tyr
XR_429316.4:n.4790C>A
NM_001080414.4:c.4664C>A MANE Select	NP_001073883.2:p.Ser1555Tyr