Canonical Allele Identifier: CA923740967

Gene: ZNF886P

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20004678_20004679insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000686.2:g.20004678_20004679insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000024.9:g.22166564_22166565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000686.1:g.22166564_22166565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000024.8:g.20625952_20625953insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450781.1:n.208+1090_208+1091insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA