Canonical Allele Identifier: CA697266605
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs779927126
MyVariant Identifiers: chr13:g.31337928C>G (hg19) chr13:g.30763791C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30763791C>G , CM000675.2:g.30763791C>G GRCh38
NC_000013.10:g.31337928C>G , CM000675.1:g.31337928C>G GRCh37
NC_000013.9:g.30235928C>G NCBI36
NG_011963.2:g.55314C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380490.5:c.324-153C>G MANE Select ENSP00000369858.3:n.324-153C>G
ENST00000380490.4:c.324-153C>G ENSP00000369858.3:n.324-153C>G
ENST00000617770.4:c.495-153C>G ENSP00000479870.1:n.495-153C>G
NM_001204406.1:c.495-153C>G NP_001191335.1:n.495-153C>G
NM_001629.3:c.324-153C>G NP_001620.2:n.324-153C>G
XM_011535025.1:c.204-153C>G XP_011533327.1:n.204-153C>G
XM_017020522.2:c.204-153C>G XP_016876011.1:n.204-153C>G
NM_001204406.2:c.495-153C>G NP_001191335.1:n.495-153C>G
NM_001629.4:c.324-153C>G MANE Select NP_001620.2:n.324-153C>G
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