Canonical Allele Identifier: CA2154899611
Gene: CCDC88C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272364A= , CM000676.2:g.91272364A= GRCh38
NC_000014.8:g.91738708A= , CM000676.1:g.91738708A= GRCh37
NC_000014.7:g.90808461A= NCBI36
NG_033118.1:g.150481T=
NG_033118.2:g.150481T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*261T= MANE Select ENSP00000374507.6:n.*261T=
ENST00000331194.8:c.*261T= ENSP00000330332.8:n.*261T=
ENST00000389857.10:c.*261T= ENSP00000374507.6:n.*261T=
ENST00000556726.5:c.2576T=
NM_001080414.3:c.*261T= NP_001073883.2:n.*261T=
XM_011536796.1:c.*261T= XP_011535098.1:n.*261T=
XM_011536796.2:c.*261T= XP_011535098.1:n.*261T=
XM_017021336.1:c.*261T= XP_016876825.1:n.*261T=
NM_001080414.4:c.*261T= MANE Select NP_001073883.2:n.*261T=
Search 100 bp 5'
Search 100 bp 3'