Canonical Allele Identifier: CA390610846

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739941A>T (hg19) ; chr14:g.91273597A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273597A>T , CM000676.2:g.91273597A>T	GRCh38
NC_000014.8:g.91739941A>T , CM000676.1:g.91739941A>T	GRCh37
NC_000014.7:g.90809694A>T	NCBI36
NG_033118.1:g.149248T>A
NG_033118.2:g.149248T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5115T>A MANE Select	ENSP00000374507.6:p.Asp1705Glu
ENST00000331194.8:c.687T>A	ENSP00000330332.8:p.Asp229Glu
ENST00000334448.5:n.927T>A
ENST00000389857.10:c.5115T>A	ENSP00000374507.6:p.Asp1705Glu
ENST00000556726.5:c.1343T>A
NM_001080414.3:c.5115T>A	NP_001073883.2:p.Asp1705Glu
XM_011536796.1:c.5007T>A	XP_011535098.1:p.Asp1669Glu
XR_429316.2:n.5390T>A
XM_011536796.2:c.5007T>A	XP_011535098.1:p.Asp1669Glu
XM_017021336.1:c.2196T>A	XP_016876825.1:p.Asp732Glu
XR_429316.4:n.5388T>A
NM_001080414.4:c.5115T>A MANE Select	NP_001073883.2:p.Asp1705Glu