Canonical Allele Identifier: CA954573110
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1951738366

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30738557A>G , CM000675.2:g.30738557A>G GRCh38
NC_000013.10:g.31312694A>G , CM000675.1:g.31312694A>G GRCh37
NC_000013.9:g.30210694A>G NCBI36
NG_011963.2:g.30080A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380490.5:c.70+2882A>G MANE Select ENSP00000369858.3:n.70+2882A>G
ENST00000380490.4:c.70+2882A>G ENSP00000369858.3:n.70+2882A>G
ENST00000617770.4:c.241+2882A>G ENSP00000479870.1:n.241+2882A>G
NM_001204406.1:c.241+2882A>G NP_001191335.1:n.241+2882A>G
NM_001629.3:c.70+2882A>G NP_001620.2:n.70+2882A>G
XM_011535024.1:c.70+2882A>G XP_011533326.1:n.70+2882A>G
NM_001204406.2:c.241+2882A>G NP_001191335.1:n.241+2882A>G
NM_001629.4:c.70+2882A>G MANE Select NP_001620.2:n.70+2882A>G