Canonical Allele Identifier: CA487541312

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91804493C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338149C>A , CM000676.2:g.91338149C>A	GRCh38
NC_000014.8:g.91804493C>A , CM000676.1:g.91804493C>A	GRCh37
NC_000014.7:g.90874246C>A	NCBI36
NG_033118.1:g.84696G>T
NG_033118.2:g.84696G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.906G>T MANE Select	ENSP00000374507.6:p.Ala302=
ENST00000389857.10:c.906G>T	ENSP00000374507.6:p.Ala302=
ENST00000554051.1:n.383G>T
NM_001080414.3:c.906G>T	NP_001073883.2:p.Ala302=
XM_005267691.3:c.906G>T	XP_005267748.1:p.Ala302=
XM_011536796.1:c.798G>T	XP_011535098.1:p.Ala266=
XR_429316.2:n.1034G>T
XR_943459.1:n.1034G>T
XM_005267691.5:c.906G>T	XP_005267748.1:p.Ala302=
XM_011536796.2:c.798G>T	XP_011535098.1:p.Ala266=
XM_017021335.2:c.906G>T	XP_016876824.1:p.Ala302=
XM_017021337.2:c.906G>T	XP_016876826.1:p.Ala302=
XR_429316.4:n.1032G>T
NM_001080414.4:c.906G>T MANE Select	NP_001073883.2:p.Ala302=