Canonical Allele Identifier: CA2154900118
Gene: CCDC88C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272694_91272696delinsCTT , CM000676.2:g.91272694_91272696delinsCTT GRCh38
NC_000014.8:g.91739038_91739040delinsCTT , CM000676.1:g.91739038_91739040delinsCTT GRCh37
NC_000014.7:g.90808791_90808793delinsCTT NCBI36
NG_033118.1:g.150149_150151delinsAAG
NG_033118.2:g.150149_150151delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.6016_6018delinsAAG MANE Select ENSP00000374507.6:p.Lys2006=
ENST00000331194.8:c.1450_1452delinsAAG ENSP00000330332.8:p.Lys484=
ENST00000389857.10:c.6016_6018delinsAAG ENSP00000374507.6:p.Lys2006=
ENST00000556726.5:c.2244_2246delinsAAG
NM_001080414.3:c.6016_6018delinsAAG NP_001073883.2:p.Lys2006=
XM_011536796.1:c.5908_5910delinsAAG XP_011535098.1:p.Lys1970=
XM_011536796.2:c.5908_5910delinsAAG XP_011535098.1:p.Lys1970=
XM_017021336.1:c.3097_3099delinsAAG XP_016876825.1:p.Lys1033=
NM_001080414.4:c.6016_6018delinsAAG MANE Select NP_001073883.2:p.Lys2006=
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