Canonical Allele Identifier: CA487541204

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91804420T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338076T>G , CM000676.2:g.91338076T>G	GRCh38
NC_000014.8:g.91804420T>G , CM000676.1:g.91804420T>G	GRCh37
NC_000014.7:g.90874173T>G	NCBI36
NG_033118.1:g.84769A>C
NG_033118.2:g.84769A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.979A>C MANE Select	ENSP00000374507.6:p.Arg327=
ENST00000389857.10:c.979A>C	ENSP00000374507.6:p.Arg327=
ENST00000554051.1:n.456A>C
NM_001080414.3:c.979A>C	NP_001073883.2:p.Arg327=
XM_005267691.3:c.979A>C	XP_005267748.1:p.Arg327=
XM_011536796.1:c.871A>C	XP_011535098.1:p.Arg291=
XR_429316.2:n.1107A>C
XR_943459.1:n.1107A>C
XM_005267691.5:c.979A>C	XP_005267748.1:p.Arg327=
XM_011536796.2:c.871A>C	XP_011535098.1:p.Arg291=
XM_017021335.2:c.979A>C	XP_016876824.1:p.Arg327=
XM_017021337.2:c.979A>C	XP_016876826.1:p.Arg327=
XR_429316.4:n.1105A>C
NM_001080414.4:c.979A>C MANE Select	NP_001073883.2:p.Arg327=