Canonical Allele Identifier: CA390610611

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739827C>A (hg19) ; chr14:g.91273483C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273483C>A , CM000676.2:g.91273483C>A	GRCh38
NC_000014.8:g.91739827C>A , CM000676.1:g.91739827C>A	GRCh37
NC_000014.7:g.90809580C>A	NCBI36
NG_033118.1:g.149362G>T
NG_033118.2:g.149362G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5229G>T MANE Select	ENSP00000374507.6:p.Arg1743Ser
ENST00000331194.8:c.801G>T	ENSP00000330332.8:p.Arg267Ser
ENST00000334448.5:n.1041G>T
ENST00000389857.10:c.5229G>T	ENSP00000374507.6:p.Arg1743Ser
ENST00000556726.5:c.1457G>T
NM_001080414.3:c.5229G>T	NP_001073883.2:p.Arg1743Ser
XM_011536796.1:c.5121G>T	XP_011535098.1:p.Arg1707Ser
XR_429316.2:n.5504G>T
XM_011536796.2:c.5121G>T	XP_011535098.1:p.Arg1707Ser
XM_017021336.1:c.2310G>T	XP_016876825.1:p.Arg770Ser
XR_429316.4:n.5502G>T
NM_001080414.4:c.5229G>T MANE Select	NP_001073883.2:p.Arg1743Ser