Canonical Allele Identifier: CA2082069321
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730954_30730958delinsTCTAA , CM000675.2:g.30730954_30730958delinsTCTAA GRCh38
NC_000013.10:g.31305091_31305095delinsTCTAA , CM000675.1:g.31305091_31305095delinsTCTAA GRCh37
NC_000013.9:g.30203091_30203095delinsTCTAA NCBI36
NG_011963.2:g.22477_22481delinsTCTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4597_117-4593delinsTCTAA ENSP00000479870.1:n.117-4597_117-4593delinsTCTAA
NM_001204406.1:c.117-4597_117-4593delinsTCTAA NP_001191335.1:n.117-4597_117-4593delinsTCTAA
NM_001204406.2:c.117-4597_117-4593delinsTCTAA NP_001191335.1:n.117-4597_117-4593delinsTCTAA