Canonical Allele Identifier: CA390611828

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91804425A>T (hg19) ; chr14:g.91338081A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338081A>T , CM000676.2:g.91338081A>T	GRCh38
NC_000014.8:g.91804425A>T , CM000676.1:g.91804425A>T	GRCh37
NC_000014.7:g.90874178A>T	NCBI36
NG_033118.1:g.84764T>A
NG_033118.2:g.84764T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.974T>A MANE Select	ENSP00000374507.6:p.Val325Glu
ENST00000389857.10:c.974T>A	ENSP00000374507.6:p.Val325Glu
ENST00000554051.1:n.451T>A
NM_001080414.3:c.974T>A	NP_001073883.2:p.Val325Glu
XM_005267691.3:c.974T>A	XP_005267748.1:p.Val325Glu
XM_011536796.1:c.866T>A	XP_011535098.1:p.Val289Glu
XR_429316.2:n.1102T>A
XR_943459.1:n.1102T>A
XM_005267691.5:c.974T>A	XP_005267748.1:p.Val325Glu
XM_011536796.2:c.866T>A	XP_011535098.1:p.Val289Glu
XM_017021335.2:c.974T>A	XP_016876824.1:p.Val325Glu
XM_017021337.2:c.974T>A	XP_016876826.1:p.Val325Glu
XR_429316.4:n.1100T>A
NM_001080414.4:c.974T>A MANE Select	NP_001073883.2:p.Val325Glu