Canonical Allele Identifier: CA2202178781
Gene: ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340770_2340771delinsCG , CM000678.2:g.2340770_2340771delinsCG GRCh38
NC_000016.9:g.2390771_2390772delinsCG , CM000678.1:g.2390771_2390772delinsCG GRCh37
NC_000016.8:g.2330772_2330773delinsCG NCBI36
NG_011790.1:g.4976_4977delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1439_42+1440delinsCG
ENST00000512848.5:n.182+1439_182+1440delinsCG