Canonical Allele Identifier: CA390608132

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91272735-C-A
• MyVariant Identifiers: chr14:g.91739079C>A (hg19) ; chr14:g.91272735C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272735C>A , CM000676.2:g.91272735C>A	GRCh38
NC_000014.8:g.91739079C>A , CM000676.1:g.91739079C>A	GRCh37
NC_000014.7:g.90808832C>A	NCBI36
NG_033118.1:g.150110G>T
NG_033118.2:g.150110G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5977G>T MANE Select	ENSP00000374507.6:p.Gly1993Cys
ENST00000331194.8:c.1411G>T	ENSP00000330332.8:p.Gly471Cys
ENST00000389857.10:c.5977G>T	ENSP00000374507.6:p.Gly1993Cys
ENST00000556726.5:c.2205G>T
NM_001080414.3:c.5977G>T	NP_001073883.2:p.Gly1993Cys
XM_011536796.1:c.5869G>T	XP_011535098.1:p.Gly1957Cys
XM_011536796.2:c.5869G>T	XP_011535098.1:p.Gly1957Cys
XM_017021336.1:c.3058G>T	XP_016876825.1:p.Gly1020Cys
NM_001080414.4:c.5977G>T MANE Select	NP_001073883.2:p.Gly1993Cys