Canonical Allele Identifier: CA265517326

Gene: CCDC88C

Linked Data

• dbSNP Id: rs35067609
• MyVariant Identifiers: chr14:g.91739122_91739123insG (hg19) ; chr14:g.91272778_91272779insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272780dup , CM000676.2:g.91272780dup	GRCh38
NC_000014.8:g.91739124dup , CM000676.1:g.91739124dup	GRCh37
NC_000014.7:g.90808877dup	NCBI36
NG_033118.1:g.150066dup
NG_033118.2:g.150066dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5933dup MANE Select	ENSP00000374507.6:p.Ala1979GlyfsTer?
ENST00000331194.8:c.1367dup	ENSP00000330332.8:p.Ala457GlyfsTer?
ENST00000389857.10:c.5933dup	ENSP00000374507.6:p.Ala1979GlyfsTer?
ENST00000556726.5:c.2161dup
NM_001080414.3:c.5933dup	NP_001073883.2:p.Ala1979GlyfsTer?
XM_011536796.1:c.5825dup	XP_011535098.1:p.Ala1943GlyfsTer?
XM_011536796.2:c.5825dup	XP_011535098.1:p.Ala1943GlyfsTer?
XM_017021336.1:c.3014dup	XP_016876825.1:p.Ala1006GlyfsTer?
NM_001080414.4:c.5933dup MANE Select	NP_001073883.2:p.Ala1979GlyfsTer?