Canonical Allele Identifier: CA2154879114
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91313604_91313607delinsCCTT , CM000676.2:g.91313604_91313607delinsCCTT GRCh38
NC_000014.8:g.91779948_91779951delinsCCTT , CM000676.1:g.91779948_91779951delinsCCTT GRCh37
NC_000014.7:g.90849701_90849704delinsCCTT NCBI36
NG_033118.1:g.109238_109241delinsAAGG
NG_033118.2:g.109238_109241delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.2209_2212delinsAAGG MANE Select ENSP00000374507.6:p.Lys737=
ENST00000389857.10:c.2209_2212delinsAAGG ENSP00000374507.6:p.Lys737=
NM_001080414.3:c.2209_2212delinsAAGG NP_001073883.2:p.Lys737=
XM_005267691.3:c.2209_2212delinsAAGG XP_005267748.1:p.Lys737=
XM_011536796.1:c.2101_2104delinsAAGG XP_011535098.1:p.Lys701=
XR_429316.2:n.2337_2340delinsAAGG
XR_943459.1:n.2337_2340delinsAAGG
XM_005267691.5:c.2209_2212delinsAAGG XP_005267748.1:p.Lys737=
XM_011536796.2:c.2101_2104delinsAAGG XP_011535098.1:p.Lys701=
XM_017021335.2:c.2209_2212delinsAAGG XP_016876824.1:p.Lys737=
XM_017021337.2:c.2209_2212delinsAAGG XP_016876826.1:p.Lys737=
XR_429316.4:n.2335_2338delinsAAGG
NM_001080414.4:c.2209_2212delinsAAGG MANE Select NP_001073883.2:p.Lys737=