Canonical Allele Identifier: CA487541253

Gene: CCDC88C

Linked Data

• COSMIC: COSM1237075 ; COSM1237076
• MyVariant Identifiers: chr14:g.91804454C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338110C>A , CM000676.2:g.91338110C>A	GRCh38
NC_000014.8:g.91804454C>A , CM000676.1:g.91804454C>A	GRCh37
NC_000014.7:g.90874207C>A	NCBI36
NG_033118.1:g.84735G>T
NG_033118.2:g.84735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.945G>T MANE Select	ENSP00000374507.6:p.Leu315=
ENST00000389857.10:c.945G>T	ENSP00000374507.6:p.Leu315=
ENST00000554051.1:n.422G>T
NM_001080414.3:c.945G>T	NP_001073883.2:p.Leu315=
XM_005267691.3:c.945G>T	XP_005267748.1:p.Leu315=
XM_011536796.1:c.837G>T	XP_011535098.1:p.Leu279=
XR_429316.2:n.1073G>T
XR_943459.1:n.1073G>T
XM_005267691.5:c.945G>T	XP_005267748.1:p.Leu315=
XM_011536796.2:c.837G>T	XP_011535098.1:p.Leu279=
XM_017021335.2:c.945G>T	XP_016876824.1:p.Leu315=
XM_017021337.2:c.945G>T	XP_016876826.1:p.Leu315=
XR_429316.4:n.1071G>T
NM_001080414.4:c.945G>T MANE Select	NP_001073883.2:p.Leu315=