Canonical Allele Identifier: CA487829176

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739982G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273638G>T , CM000676.2:g.91273638G>T	GRCh38
NC_000014.8:g.91739982G>T , CM000676.1:g.91739982G>T	GRCh37
NC_000014.7:g.90809735G>T	NCBI36
NG_033118.1:g.149207C>A
NG_033118.2:g.149207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5074C>A MANE Select	ENSP00000374507.6:p.Arg1692=
ENST00000331194.8:c.646C>A	ENSP00000330332.8:p.Arg216=
ENST00000334448.5:n.886C>A
ENST00000389857.10:c.5074C>A	ENSP00000374507.6:p.Arg1692=
ENST00000556726.5:c.1302C>A
NM_001080414.3:c.5074C>A	NP_001073883.2:p.Arg1692=
XM_011536796.1:c.4966C>A	XP_011535098.1:p.Arg1656=
XR_429316.2:n.5349C>A
XM_011536796.2:c.4966C>A	XP_011535098.1:p.Arg1656=
XM_017021336.1:c.2155C>A	XP_016876825.1:p.Arg719=
XR_429316.4:n.5347C>A
NM_001080414.4:c.5074C>A MANE Select	NP_001073883.2:p.Arg1692=