Canonical Allele Identifier: CA487829303

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91273492-C-A
• MyVariant Identifiers: chr14:g.91739836C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273492C>A , CM000676.2:g.91273492C>A	GRCh38
NC_000014.8:g.91739836C>A , CM000676.1:g.91739836C>A	GRCh37
NC_000014.7:g.90809589C>A	NCBI36
NG_033118.1:g.149353G>T
NG_033118.2:g.149353G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5220G>T MANE Select	ENSP00000374507.6:p.Ser1740=
ENST00000331194.8:c.792G>T	ENSP00000330332.8:p.Ser264=
ENST00000334448.5:n.1032G>T
ENST00000389857.10:c.5220G>T	ENSP00000374507.6:p.Ser1740=
ENST00000556726.5:c.1448G>T
NM_001080414.3:c.5220G>T	NP_001073883.2:p.Ser1740=
XM_011536796.1:c.5112G>T	XP_011535098.1:p.Ser1704=
XR_429316.2:n.5495G>T
XM_011536796.2:c.5112G>T	XP_011535098.1:p.Ser1704=
XM_017021336.1:c.2301G>T	XP_016876825.1:p.Ser767=
XR_429316.4:n.5493G>T
NM_001080414.4:c.5220G>T MANE Select	NP_001073883.2:p.Ser1740=