Canonical Allele Identifier: CA2202178788
Gene: ABCA17P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340772_2340774delinsGAT , CM000678.2:g.2340772_2340774delinsGAT GRCh38
NC_000016.9:g.2390773_2390775delinsGAT , CM000678.1:g.2390773_2390775delinsGAT GRCh37
NC_000016.8:g.2330774_2330776delinsGAT NCBI36
NG_011790.1:g.4973_4975delinsATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1441_42+1443delinsGAT
ENST00000512848.5:n.182+1441_182+1443delinsGAT
Search 100 bp 5'
Search 100 bp 3'