Canonical Allele Identifier: CA7309026

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91289162C>T , CM000676.2:g.91289162C>T	GRCh38
NC_000014.8:g.91755506C>T , CM000676.1:g.91755506C>T	GRCh37
NC_000014.7:g.90825259C>T	NCBI36
NG_033118.1:g.133683G>A
NG_033118.2:g.133683G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001080414.4:c.4384G>A MANE Select	NP_001073883.2:p.Ala1462Thr
ENST00000389857.11:c.4384G>A MANE Select	ENSP00000374507.6:p.Ala1462Thr
NM_001080414.3:c.4384G>A	NP_001073883.2:p.Ala1462Thr
ENST00000389857.10:c.4384G>A	ENSP00000374507.6:p.Ala1462Thr
ENST00000555995.1:n.259G>A
ENST00000556726.5:c.170G>A
XM_005267691.3:c.4384G>A	XP_005267748.1:p.Ala1462Thr
XM_005267691.5:c.4384G>A	XP_005267748.1:p.Ala1462Thr
XM_011536796.1:c.4276G>A	XP_011535098.1:p.Ala1426Thr
XM_011536796.2:c.4276G>A	XP_011535098.1:p.Ala1426Thr
XM_017021335.2:c.4384G>A	XP_016876824.1:p.Ala1462Thr
XM_017021336.1:c.1465G>A	XP_016876825.1:p.Ala489Thr
XR_429316.2:n.4512G>A
XR_429316.4:n.4510G>A
XR_943459.1:n.4512G>A