Canonical Allele Identifier: CA2154899807
Gene: CCDC88C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272539G= , CM000676.2:g.91272539G= GRCh38
NC_000014.8:g.91738883G= , CM000676.1:g.91738883G= GRCh37
NC_000014.7:g.90808636G= NCBI36
NG_033118.1:g.150306C=
NG_033118.2:g.150306C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*86C= MANE Select ENSP00000374507.6:n.*86C=
ENST00000331194.8:c.*86C= ENSP00000330332.8:n.*86C=
ENST00000389857.10:c.*86C= ENSP00000374507.6:n.*86C=
ENST00000556726.5:c.2401C=
NM_001080414.3:c.*86C= NP_001073883.2:n.*86C=
XM_011536796.1:c.*86C= XP_011535098.1:n.*86C=
XM_011536796.2:c.*86C= XP_011535098.1:n.*86C=
XM_017021336.1:c.*86C= XP_016876825.1:n.*86C=
NM_001080414.4:c.*86C= MANE Select NP_001073883.2:n.*86C=
Search 100 bp 5'
Search 100 bp 3'