Canonical Allele Identifier: CA390610136

Gene: CCDC88C

Linked Data

• ClinVar Variation Id: 2829133
• ClinVar RCV Id: RCV003693992
• gnomAD v4: 14-91273404-G-A
• MyVariant Identifiers: chr14:g.91739748G>A (hg19) ; chr14:g.91273404G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273404G>A , CM000676.2:g.91273404G>A	GRCh38
NC_000014.8:g.91739748G>A , CM000676.1:g.91739748G>A	GRCh37
NC_000014.7:g.90809501G>A	NCBI36
NG_033118.1:g.149441C>T
NG_033118.2:g.149441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5308C>T MANE Select	ENSP00000374507.6:p.Gln1770Ter
ENST00000331194.8:c.880C>T	ENSP00000330332.8:p.Gln294Ter
ENST00000389857.10:c.5308C>T	ENSP00000374507.6:p.Gln1770Ter
ENST00000556726.5:c.1536C>T
NM_001080414.3:c.5308C>T	NP_001073883.2:p.Gln1770Ter
XM_011536796.1:c.5200C>T	XP_011535098.1:p.Gln1734Ter
XM_011536796.2:c.5200C>T	XP_011535098.1:p.Gln1734Ter
XM_017021336.1:c.2389C>T	XP_016876825.1:p.Gln797Ter
NM_001080414.4:c.5308C>T MANE Select	NP_001073883.2:p.Gln1770Ter