Canonical Allele Identifier: CA487829385

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739962G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273618G>A , CM000676.2:g.91273618G>A	GRCh38
NC_000014.8:g.91739962G>A , CM000676.1:g.91739962G>A	GRCh37
NC_000014.7:g.90809715G>A	NCBI36
NG_033118.1:g.149227C>T
NG_033118.2:g.149227C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5094C>T MANE Select	ENSP00000374507.6:p.Asp1698=
ENST00000331194.8:c.666C>T	ENSP00000330332.8:p.Asp222=
ENST00000334448.5:n.906C>T
ENST00000389857.10:c.5094C>T	ENSP00000374507.6:p.Asp1698=
ENST00000556726.5:c.1322C>T
NM_001080414.3:c.5094C>T	NP_001073883.2:p.Asp1698=
XM_011536796.1:c.4986C>T	XP_011535098.1:p.Asp1662=
XR_429316.2:n.5369C>T
XM_011536796.2:c.4986C>T	XP_011535098.1:p.Asp1662=
XM_017021336.1:c.2175C>T	XP_016876825.1:p.Asp725=
XR_429316.4:n.5367C>T
NM_001080414.4:c.5094C>T MANE Select	NP_001073883.2:p.Asp1698=