Canonical Allele Identifier: CA2622555849

Gene: ALOX5AP

Linked Data

• gnomAD v4: 13-30763802-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30763802A>G , CM000675.2:g.30763802A>G	GRCh38
NC_000013.10:g.31337939A>G , CM000675.1:g.31337939A>G	GRCh37
NC_000013.9:g.30235939A>G	NCBI36
NG_011963.2:g.55325A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380490.5:c.324-142A>G MANE Select	ENSP00000369858.3:n.324-142A>G
ENST00000380490.4:c.324-142A>G	ENSP00000369858.3:n.324-142A>G
ENST00000617770.4:c.495-142A>G	ENSP00000479870.1:n.495-142A>G
NM_001204406.1:c.495-142A>G	NP_001191335.1:n.495-142A>G
NM_001629.3:c.324-142A>G	NP_001620.2:n.324-142A>G
XM_011535025.1:c.204-142A>G	XP_011533327.1:n.204-142A>G
XM_017020522.2:c.204-142A>G	XP_016876011.1:n.204-142A>G
NM_001204406.2:c.495-142A>G	NP_001191335.1:n.495-142A>G
NM_001629.4:c.324-142A>G MANE Select	NP_001620.2:n.324-142A>G