Canonical Allele Identifier: CA2202178761
Gene: ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340760_2340781delinsGGGGGCGCCGCGGATGGCGCGT , CM000678.2:g.2340760_2340781delinsGGGGGCGCCGCGGATGGCGCGT GRCh38
NC_000016.9:g.2390761_2390782delinsGGGGGCGCCGCGGATGGCGCGT , CM000678.1:g.2390761_2390782delinsGGGGGCGCCGCGGATGGCGCGT GRCh37
NC_000016.8:g.2330762_2330783delinsGGGGGCGCCGCGGATGGCGCGT NCBI36
NG_011790.1:g.4966_4987delinsACGCGCCATCCGCGGCGCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1429_42+1450delinsGGGGGCGCCGCGGATGGCGCGT
ENST00000512848.5:n.182+1429_182+1450delinsGGGGGCGCCGCGGATGGCGCGT